Canonical Allele Identifier: CA2838381589

Gene: CCDC17

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45623495A>G , CM000663.2:g.45623495A>G	GRCh38
NC_000001.10:g.46089167A>G , CM000663.1:g.46089167A>G	GRCh37
NC_000001.9:g.45861754A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528266.6:c.271-56T>C MANE Select	ENSP00000432172.1:n.271-56T>C
ENST00000372044.7:c.174+241T>C	ENSP00000361114.3:n.174+241T>C
ENST00000421127.6:c.270+62T>C	ENSP00000389415.2:n.270+62T>C
ENST00000445048.2:c.174+241T>C	ENSP00000411335.2:n.174+241T>C
ENST00000479529.2:c.175-56T>C	ENSP00000437072.1:n.175-56T>C
ENST00000482416.5:n.543T>C
ENST00000491755.5:n.463T>C
ENST00000525599.1:n.472T>C
ENST00000528266.5:c.271-56T>C	ENSP00000432172.1:n.271-56T>C
NM_001114938.2:c.271-56T>C	NP_001108410.2:n.271-56T>C
NM_001190182.1:c.270+62T>C	NP_001177111.1:n.270+62T>C
XM_011540806.1:c.271-56T>C	XP_011539108.1:n.271-56T>C
XM_011540807.1:c.270+62T>C	XP_011539109.1:n.270+62T>C
XM_011540808.1:c.271-56T>C	XP_011539110.1:n.271-56T>C
XM_011540809.1:c.175-56T>C	XP_011539111.1:n.175-56T>C
XM_011540810.1:c.271-56T>C	XP_011539112.1:n.271-56T>C
XM_011540811.1:c.175-83T>C	XP_011539113.1:n.175-83T>C
XM_011540812.1:c.271-56T>C	XP_011539114.1:n.271-56T>C
XM_011540813.1:c.175-56T>C	XP_011539115.1:n.175-56T>C
XM_011540814.1:c.271-56T>C	XP_011539116.1:n.271-56T>C
XM_011540815.1:c.-86T>C	XP_011539117.1:n.-86T>C
XM_011540816.1:c.271-56T>C	XP_011539118.1:n.271-56T>C
XM_011540817.1:c.-45+62T>C	XP_011539119.1:n.-45+62T>C
XM_011540818.1:c.-45+241T>C	XP_011539120.1:n.-45+241T>C
XM_011540819.1:c.-45+98T>C	XP_011539121.1:n.-45+98T>C
XM_011540820.1:c.271-56T>C	XP_011539122.1:n.271-56T>C
XR_946555.1:n.1149-56T>C
XR_946556.1:n.319-56T>C
XM_017000450.1:c.270+62T>C	XP_016855939.1:n.270+62T>C
XM_017000451.1:c.175-56T>C	XP_016855940.1:n.175-56T>C
XM_017000452.1:c.271-56T>C	XP_016855941.1:n.271-56T>C
XM_017000453.1:c.271-56T>C	XP_016855942.1:n.271-56T>C
XM_017000454.1:c.175-56T>C	XP_016855943.1:n.175-56T>C
XM_017000455.1:c.-45+241T>C	XP_016855944.1:n.-45+241T>C
XM_017000456.1:c.-45+62T>C	XP_016855945.1:n.-45+62T>C
XM_017000457.1:c.271-56T>C	XP_016855946.1:n.271-56T>C
XM_017000458.1:c.271-56T>C	XP_016855947.1:n.271-56T>C
XR_001736998.1:n.1149-56T>C
NM_001114938.3:c.271-56T>C MANE Select	NP_001108410.2:n.271-56T>C
NM_001190182.2:c.270+62T>C	NP_001177111.1:n.270+62T>C