Canonical Allele Identifier: CA1932839473

Gene: CYP17A1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102835193_102835194delinsTC , CM000672.2:g.102835193_102835194delinsTC	GRCh38
NC_000010.10:g.104594950_104594951delinsTC , CM000672.1:g.104594950_104594951delinsTC	GRCh37
NC_000010.9:g.104584940_104584941delinsTC	NCBI36
NG_007955.1:g.7340_7341delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.436+60_436+61delinsGA MANE Select	ENSP00000358903.3:n.436+60_436+61delinsGA
ENST00000638190.1:c.436+60_436+61delinsGA	ENSP00000492539.1:n.436+60_436+61delinsGA
ENST00000638272.1:c.297+1871_297+1872delinsGA	ENSP00000491508.1:n.297+1871_297+1872delinsGA
ENST00000638971.1:c.436+60_436+61delinsGA	ENSP00000492313.1:n.436+60_436+61delinsGA
ENST00000639393.1:c.436+60_436+61delinsGA	ENSP00000492651.1:n.436+60_436+61delinsGA
ENST00000640633.1:n.198+60_198+61delinsGA
ENST00000369887.3:c.436+60_436+61delinsGA	ENSP00000358903.3:n.436+60_436+61delinsGA
ENST00000489268.1:n.690+60_690+61delinsGA
NM_000102.3:c.436+60_436+61delinsGA	NP_000093.1:n.436+60_436+61delinsGA
NM_000102.4:c.436+60_436+61delinsGA MANE Select	NP_000093.1:n.436+60_436+61delinsGA