Canonical Allele Identifier: CA1932839498

Gene: CYP17A1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102835211T= , CM000672.2:g.102835211T=	GRCh38
NC_000010.10:g.104594968T= , CM000672.1:g.104594968T=	GRCh37
NC_000010.9:g.104584958T=	NCBI36
NG_007955.1:g.7323A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.436+43A= MANE Select	ENSP00000358903.3:n.436+43A=
ENST00000638190.1:c.436+43A=	ENSP00000492539.1:n.436+43A=
ENST00000638272.1:c.297+1854A=	ENSP00000491508.1:n.297+1854A=
ENST00000638971.1:c.436+43A=	ENSP00000492313.1:n.436+43A=
ENST00000639393.1:c.436+43A=	ENSP00000492651.1:n.436+43A=
ENST00000640633.1:n.198+43A=
ENST00000369887.3:c.436+43A=	ENSP00000358903.3:n.436+43A=
ENST00000489268.1:n.690+43A=
NM_000102.3:c.436+43A=	NP_000093.1:n.436+43A=
NM_000102.4:c.436+43A= MANE Select	NP_000093.1:n.436+43A=