Canonical Allele Identifier: CA2808394852

Gene: CTC1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8232258_8232270del , CM000679.2:g.8232258_8232270del	GRCh38
NC_000017.10:g.8135576_8135588del , CM000679.1:g.8135576_8135588del	GRCh37
NC_000017.9:g.8076301_8076313del	NCBI36
NG_032148.1:g.20826_20838del
NG_032148.2:g.20826_20838del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000580299.2:c.2061-43_2061-31del	ENSP00000462607.2:n.2061-43_2061-31del
ENST00000581729.2:c.2061-43_2061-31del	ENSP00000462720.2:n.2061-43_2061-31del
ENST00000581967.2:n.2513-43_2513-31del
ENST00000583254.2:n.2767-43_2767-31del
ENST00000699849.1:c.1164-43_1164-31del	ENSP00000514647.1:n.1164-43_1164-31del
ENST00000699850.1:n.1324-43_1324-31del
ENST00000699851.1:n.2083-43_2083-31del
ENST00000699852.1:c.*737-43_*737-31del	ENSP00000514648.1:n.*737-43_*737-31del
ENST00000699853.1:c.2061-43_2061-31del	ENSP00000514649.1:n.2061-43_2061-31del
ENST00000699854.1:n.1854-43_1854-31del
ENST00000699855.1:n.2513-43_2513-31del
ENST00000699856.1:c.2061-43_2061-31del	ENSP00000514650.1:n.2061-43_2061-31del
ENST00000699857.1:n.2069-43_2069-31del
ENST00000699858.1:c.*674-43_*674-31del	ENSP00000514651.1:n.*674-43_*674-31del
ENST00000699859.1:c.1932-43_1932-31del	ENSP00000514652.1:n.1932-43_1932-31del
ENST00000699860.1:n.167-43_167-31del
ENST00000699861.1:n.2083-43_2083-31del
ENST00000699862.1:n.3021-43_3021-31del
ENST00000449476.7:c.1956-43_1956-31del	ENSP00000396018.2:n.1956-43_1956-31del
ENST00000581671.2:n.2050-43_2050-31del
ENST00000643543.1:c.*768-43_*768-31del	ENSP00000494323.1:n.*768-43_*768-31del
ENST00000651323.1:c.2061-43_2061-31del MANE Select	ENSP00000498499.1:n.2061-43_2061-31del
ENST00000315684.12:c.2061-43_2061-31del	ENSP00000313759.8:n.2061-43_2061-31del
ENST00000449476.6:c.1956-43_1956-31del	ENSP00000396018.2:n.1956-43_1956-31del
ENST00000578240.1:n.289-43_289-31del
NM_025099.5:c.2061-43_2061-31del	NP_079375.3:n.2061-43_2061-31del
NR_046431.1:n.2015-43_2015-31del
XM_006721577.2:c.1932-43_1932-31del	XP_006721640.1:n.1932-43_1932-31del
XM_006721578.2:c.2061-43_2061-31del	XP_006721641.1:n.2061-43_2061-31del
XM_006721579.2:c.2061-43_2061-31del	XP_006721642.1:n.2061-43_2061-31del
XM_011524010.1:c.1956-43_1956-31del	XP_011522312.1:n.1956-43_1956-31del
XM_011524011.1:c.1164-43_1164-31del	XP_011522313.1:n.1164-43_1164-31del
XR_429823.2:n.2104-43_2104-31del
XR_429824.2:n.2104-43_2104-31del
XR_429825.1:n.2104-43_2104-31del
NM_025099.6:c.2061-43_2061-31del MANE Select	NP_079375.3:n.2061-43_2061-31del
XM_006721577.3:c.1932-43_1932-31del	XP_006721640.1:n.1932-43_1932-31del
XM_006721578.3:c.2061-43_2061-31del	XP_006721641.1:n.2061-43_2061-31del
XM_011524010.2:c.1956-43_1956-31del	XP_011522312.1:n.1956-43_1956-31del
XM_011524011.2:c.1164-43_1164-31del	XP_011522313.1:n.1164-43_1164-31del
XR_001752639.1:n.1975-43_1975-31del
XR_001752640.1:n.2104-43_2104-31del
XR_001752641.1:n.2104-43_2104-31del
XR_001752642.1:n.2104-43_2104-31del
XR_001752643.1:n.2534-43_2534-31del
XR_002958073.1:n.2104-43_2104-31del
XR_429823.3:n.2104-43_2104-31del
XR_429824.3:n.2104-43_2104-31del
NR_046431.2:n.1976-43_1976-31del