Canonical Allele Identifier: CA1932839471

Gene: CYP17A1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102835191_102835193delinsCCT , CM000672.2:g.102835191_102835193delinsCCT	GRCh38
NC_000010.10:g.104594948_104594950delinsCCT , CM000672.1:g.104594948_104594950delinsCCT	GRCh37
NC_000010.9:g.104584938_104584940delinsCCT	NCBI36
NG_007955.1:g.7341_7343delinsAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.436+61_436+63delinsAGG MANE Select	ENSP00000358903.3:n.436+61_436+63delinsAGG
ENST00000638190.1:c.436+61_436+63delinsAGG	ENSP00000492539.1:n.436+61_436+63delinsAGG
ENST00000638272.1:c.297+1872_297+1874delinsAGG	ENSP00000491508.1:n.297+1872_297+1874delinsAGG
ENST00000638971.1:c.436+61_436+63delinsAGG	ENSP00000492313.1:n.436+61_436+63delinsAGG
ENST00000639393.1:c.436+61_436+63delinsAGG	ENSP00000492651.1:n.436+61_436+63delinsAGG
ENST00000640633.1:n.198+61_198+63delinsAGG
ENST00000369887.3:c.436+61_436+63delinsAGG	ENSP00000358903.3:n.436+61_436+63delinsAGG
ENST00000489268.1:n.690+61_690+63delinsAGG
NM_000102.3:c.436+61_436+63delinsAGG	NP_000093.1:n.436+61_436+63delinsAGG
NM_000102.4:c.436+61_436+63delinsAGG MANE Select	NP_000093.1:n.436+61_436+63delinsAGG