Canonical Allele Identifier: CA377938706

Gene: CYP17A1 WBP1L

Linked Data

• gnomAD v4: 10-102832535-G-T
• MyVariant Identifiers: chr10:g.104592292G>T (hg19) ; chr10:g.102832535G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102832535G>T , CM000672.2:g.102832535G>T	GRCh38
NC_000010.10:g.104592292G>T , CM000672.1:g.104592292G>T	GRCh37
NC_000010.9:g.104582282G>T	NCBI36
NG_007955.1:g.9999C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000369887.4:c.1115C>A (CYP17A1) MANE Select	ENSP00000358903.3:p.Pro372His
ENST00000638190.1:c.812C>A (CYP17A1)	ENSP00000492539.1:p.Pro271His
ENST00000638272.1:c.659C>A (CYP17A1)	ENSP00000491508.1:p.Pro220His
ENST00000638971.1:c.1028C>A (CYP17A1)	ENSP00000492313.1:p.Pro343His
ENST00000639393.1:c.1115C>A (CYP17A1)	ENSP00000492651.1:p.Pro372His
ENST00000640633.1:n.877C>A (CYP17A1)
ENST00000647664.1:c.*1566G>T (WBP1L)	ENSP00000498131.1:n.*1566G>T
ENST00000369887.3:c.1115C>A (CYP17A1)	ENSP00000358903.3:p.Pro372His
NM_000102.3:c.1115C>A (CYP17A1)	NP_000093.1:p.Pro372His
NM_000102.4:c.1115C>A (CYP17A1) MANE Select	NP_000093.1:p.Pro372His