Canonical Allele Identifier: CA377939012

Gene: CYP17A1 WBP1L CYP17A1-AS1

Linked Data

• MyVariant Identifiers: chr10:g.104592436A>C (hg19) ; chr10:g.102832679A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102832679A>C , CM000672.2:g.102832679A>C	GRCh38
NC_000010.10:g.104592436A>C , CM000672.1:g.104592436A>C	GRCh37
NC_000010.9:g.104582426A>C	NCBI36
NG_007955.1:g.9855T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.971T>G (CYP17A1) MANE Select	ENSP00000358903.3:p.Val324Gly
ENST00000638190.1:c.668T>G (CYP17A1)	ENSP00000492539.1:p.Val223Gly
ENST00000638272.1:c.515T>G (CYP17A1)	ENSP00000491508.1:p.Val172Gly
ENST00000638971.1:c.884T>G (CYP17A1)	ENSP00000492313.1:p.Val295Gly
ENST00000639393.1:c.971T>G (CYP17A1)	ENSP00000492651.1:p.Val324Gly
ENST00000640633.1:n.733T>G (CYP17A1)
ENST00000647664.1:c.*1710A>C (WBP1L)	ENSP00000498131.1:n.*1710A>C
ENST00000369887.3:c.971T>G (CYP17A1)	ENSP00000358903.3:p.Val324Gly
NM_000102.3:c.971T>G (CYP17A1)	NP_000093.1:p.Val324Gly
XR_428804.1:n.13A>C (CYP17A1-AS1)
NM_000102.4:c.971T>G (CYP17A1) MANE Select	NP_000093.1:p.Val324Gly