Canonical Allele Identifier: CA918638729

Gene: CCDC7

Linked Data

• dbSNP Id: rs1591804448

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.32704273_32704281del , CM000672.2:g.32704273_32704281del	GRCh38
NC_000010.10:g.32993201_32993209del , CM000672.1:g.32993201_32993209del	GRCh37
NC_000010.9:g.33033207_33033215del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375028.9:c.288-7347_288-7339del
ENST00000639629.2:c.2459-7347_2459-7339del MANE Select	ENSP00000491655.1:n.2459-7347_2459-7339del
ENST00000302316.12:c.378-7347_378-7339del
ENST00000375025.10:c.853-7347_853-7339del
ENST00000375028.8:c.288-7347_288-7339del
ENST00000639290.1:n.1022-7347_1022-7339del
ENST00000639629.1:c.2459-7347_2459-7339del	ENSP00000491655.1:n.2459-7347_2459-7339del
ENST00000302316.10:c.288-7347_288-7339del
ENST00000375025.8:c.380-7347_380-7339del	ENSP00000364165.5:n.380-7347_380-7339del
ENST00000375028.6:c.308-7347_308-7339del	ENSP00000364168.3:n.308-7347_308-7339del
ENST00000375030.6:c.404-7347_404-7339del	ENSP00000364170.2:n.404-7347_404-7339del
NM_024688.2:c.380-7347_380-7339del	NP_078964.2:n.380-7347_380-7339del
XM_005252593.2:c.380-7347_380-7339del	XP_005252650.1:n.380-7347_380-7339del
XM_006717504.1:c.2459-7347_2459-7339del	XP_006717567.1:n.2459-7347_2459-7339del
XM_006717505.1:c.2246-7347_2246-7339del	XP_006717568.1:n.2246-7347_2246-7339del
XM_006717506.1:c.2138-7347_2138-7339del	XP_006717569.1:n.2138-7347_2138-7339del
XM_011519663.1:c.2459-7347_2459-7339del	XP_011517965.1:n.2459-7347_2459-7339del
XM_011519664.1:c.2459-7347_2459-7339del	XP_011517966.1:n.2459-7347_2459-7339del
XM_011519665.1:c.2438-7347_2438-7339del	XP_011517967.1:n.2438-7347_2438-7339del
XM_011519666.1:c.2459-7347_2459-7339del	XP_011517968.1:n.2459-7347_2459-7339del
XM_011519667.1:c.2459-7347_2459-7339del	XP_011517969.1:n.2459-7347_2459-7339del
XM_011519668.1:c.2369-7347_2369-7339del	XP_011517970.1:n.2369-7347_2369-7339del
XM_011519669.1:c.2357-7347_2357-7339del	XP_011517971.1:n.2357-7347_2357-7339del
XM_011519670.1:c.2351-7347_2351-7339del	XP_011517972.1:n.2351-7347_2351-7339del
XM_011519671.1:c.2459-7347_2459-7339del	XP_011517973.1:n.2459-7347_2459-7339del
XM_011519672.1:c.2348-7347_2348-7339del	XP_011517974.1:n.2348-7347_2348-7339del
XM_011519673.1:c.2345-7347_2345-7339del	XP_011517975.1:n.2345-7347_2345-7339del
XM_011519674.1:c.2459-7347_2459-7339del	XP_011517976.1:n.2459-7347_2459-7339del
XM_011519675.1:c.2249-7347_2249-7339del	XP_011517977.1:n.2249-7347_2249-7339del
XM_011519676.1:c.2345-7347_2345-7339del	XP_011517978.1:n.2345-7347_2345-7339del
XM_011519677.1:c.2237-7347_2237-7339del	XP_011517979.1:n.2237-7347_2237-7339del
XM_011519678.1:c.2234-7347_2234-7339del	XP_011517980.1:n.2234-7347_2234-7339del
XM_011519679.1:c.1928-7347_1928-7339del	XP_011517981.1:n.1928-7347_1928-7339del
XM_011519680.1:c.1799-7347_1799-7339del	XP_011517982.1:n.1799-7347_1799-7339del
XM_011519681.1:c.2459-7347_2459-7339del	XP_011517983.1:n.2459-7347_2459-7339del
XM_011519682.1:c.1544-7347_1544-7339del	XP_011517984.1:n.1544-7347_1544-7339del
XM_011519683.1:c.1538-7347_1538-7339del	XP_011517985.1:n.1538-7347_1538-7339del
XM_011519684.1:c.2459-7347_2459-7339del	XP_011517986.1:n.2459-7347_2459-7339del
XM_011519685.1:c.1376-7347_1376-7339del	XP_011517987.1:n.1376-7347_1376-7339del
XM_011519686.1:c.2459-7347_2459-7339del	XP_011517988.1:n.2459-7347_2459-7339del
XM_011519687.1:c.668-7347_668-7339del	XP_011517989.1:n.668-7347_668-7339del
NM_001321115.1:c.2459-7347_2459-7339del	NP_001308044.1:n.2459-7347_2459-7339del
XM_011519680.3:c.1799-7347_1799-7339del	XP_011517982.1:n.1799-7347_1799-7339del
XM_011519683.2:c.1538-7347_1538-7339del	XP_011517985.1:n.1538-7347_1538-7339del
XM_011519684.3:c.2459-7347_2459-7339del	XP_011517986.1:n.2459-7347_2459-7339del
XM_011519686.2:c.2459-7347_2459-7339del	XP_011517988.1:n.2459-7347_2459-7339del
XM_017016638.1:c.2459-7347_2459-7339del	XP_016872127.1:n.2459-7347_2459-7339del
XM_017016639.1:c.2458+9281_2458+9289del	XP_016872128.1:n.2458+9281_2458+9289del
XM_017016640.1:c.2459-7347_2459-7339del	XP_016872129.1:n.2459-7347_2459-7339del
XM_017016641.1:c.1898-7347_1898-7339del	XP_016872130.1:n.1898-7347_1898-7339del
XM_017016642.1:c.1799-7347_1799-7339del	XP_016872131.1:n.1799-7347_1799-7339del
XM_017016643.1:c.1649-7347_1649-7339del	XP_016872132.1:n.1649-7347_1649-7339del
XM_017016644.1:c.2459-7347_2459-7339del	XP_016872133.1:n.2459-7347_2459-7339del
XM_017016646.1:c.1544-7347_1544-7339del	XP_016872135.1:n.1544-7347_1544-7339del
XM_017016647.2:c.2459-7347_2459-7339del	XP_016872136.1:n.2459-7347_2459-7339del
XM_017016648.1:c.1403-7347_1403-7339del	XP_016872137.1:n.1403-7347_1403-7339del
XM_017016649.1:c.1178-7347_1178-7339del	XP_016872138.1:n.1178-7347_1178-7339del
XM_017016652.1:c.701-7347_701-7339del	XP_016872141.1:n.701-7347_701-7339del
XM_017016653.1:c.629-7347_629-7339del	XP_016872142.1:n.629-7347_629-7339del
XM_024448165.1:c.2438-7347_2438-7339del	XP_024303933.1:n.2438-7347_2438-7339del
XM_024448166.1:c.2426-7347_2426-7339del	XP_024303934.1:n.2426-7347_2426-7339del
XM_024448167.1:c.1544-7347_1544-7339del	XP_024303935.1:n.1544-7347_1544-7339del
XM_024448168.1:c.1544-7347_1544-7339del	XP_024303936.1:n.1544-7347_1544-7339del
XM_024448169.1:c.491-7347_491-7339del	XP_024303937.1:n.491-7347_491-7339del
XM_024448170.1:c.488-7347_488-7339del	XP_024303938.1:n.488-7347_488-7339del
NM_001321115.2:c.2459-7347_2459-7339del	NP_001308044.1:n.2459-7347_2459-7339del
NM_001395015.1:c.2459-7347_2459-7339del MANE Select	NP_001381944.1:n.2459-7347_2459-7339del
NM_001395233.1:c.1174+18193_1174+18201del	NP_001382162.1:n.1174+18193_1174+18201del