Canonical Allele Identifier: CA1932839750

Gene: CYP17A1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102835427A= , CM000672.2:g.102835427A=	GRCh38
NC_000010.10:g.104595184A= , CM000672.1:g.104595184A=	GRCh37
NC_000010.9:g.104585174A=	NCBI36
NG_007955.1:g.7107T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000369887.4:c.298-35T= MANE Select	ENSP00000358903.3:n.298-35T=
ENST00000638190.1:c.298-35T=	ENSP00000492539.1:n.298-35T=
ENST00000638272.1:c.297+1638T=	ENSP00000491508.1:n.297+1638T=
ENST00000638971.1:c.298-35T=	ENSP00000492313.1:n.298-35T=
ENST00000639393.1:c.298-35T=	ENSP00000492651.1:n.298-35T=
ENST00000640633.1:n.60-35T=
ENST00000369887.3:c.298-35T=	ENSP00000358903.3:n.298-35T=
ENST00000489268.1:n.517T=
NM_000102.3:c.298-35T=	NP_000093.1:n.298-35T=
NM_000102.4:c.298-35T= MANE Select	NP_000093.1:n.298-35T=