Canonical Allele Identifier: CA377939014

Gene: CYP17A1 WBP1L CYP17A1-AS1

Linked Data

• gnomAD v4: 10-102832680-C-G
• MyVariant Identifiers: chr10:g.104592437C>G (hg19) ; chr10:g.102832680C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102832680C>G , CM000672.2:g.102832680C>G	GRCh38
NC_000010.10:g.104592437C>G , CM000672.1:g.104592437C>G	GRCh37
NC_000010.9:g.104582427C>G	NCBI36
NG_007955.1:g.9854G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.970G>C (CYP17A1) MANE Select	ENSP00000358903.3:p.Val324Leu
ENST00000638190.1:c.667G>C (CYP17A1)	ENSP00000492539.1:p.Val223Leu
ENST00000638272.1:c.514G>C (CYP17A1)	ENSP00000491508.1:p.Val172Leu
ENST00000638971.1:c.883G>C (CYP17A1)	ENSP00000492313.1:p.Val295Leu
ENST00000639393.1:c.970G>C (CYP17A1)	ENSP00000492651.1:p.Val324Leu
ENST00000640633.1:n.732G>C (CYP17A1)
ENST00000647664.1:c.*1711C>G (WBP1L)	ENSP00000498131.1:n.*1711C>G
ENST00000369887.3:c.970G>C (CYP17A1)	ENSP00000358903.3:p.Val324Leu
NM_000102.3:c.970G>C (CYP17A1)	NP_000093.1:p.Val324Leu
XR_428804.1:n.14C>G (CYP17A1-AS1)
NM_000102.4:c.970G>C (CYP17A1) MANE Select	NP_000093.1:p.Val324Leu