Canonical Allele Identifier: CA377938178

Gene: CYP17A1 WBP1L

Linked Data

• dbSNP Id: rs965644070
• gnomAD v2: 10-104590643-G-A
• gnomAD v4: 10-102830886-G-A
• MyVariant Identifiers: chr10:g.104590643G>A (hg19) ; chr10:g.102830886G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102830886G>A , CM000672.2:g.102830886G>A	GRCh38
NC_000010.10:g.104590643G>A , CM000672.1:g.104590643G>A	GRCh37
NC_000010.9:g.104580633G>A	NCBI36
NG_007955.1:g.11648C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.1343C>T (CYP17A1) MANE Select	ENSP00000358903.3:p.Ala448Val
ENST00000638190.1:c.1040C>T (CYP17A1)	ENSP00000492539.1:p.Ala347Val
ENST00000638272.1:c.887C>T (CYP17A1)	ENSP00000491508.1:p.Ala296Val
ENST00000638971.1:c.1256C>T (CYP17A1)	ENSP00000492313.1:p.Ala419Val
ENST00000639393.1:c.1346C>T (CYP17A1)	ENSP00000492651.1:p.Ala449Val
ENST00000640633.1:n.1105C>T (CYP17A1)
ENST00000647664.1:c.*568G>A (WBP1L)	ENSP00000498131.1:n.*568G>A
ENST00000369887.3:c.1343C>T (CYP17A1)	ENSP00000358903.3:p.Ala448Val
NM_000102.3:c.1343C>T (CYP17A1)	NP_000093.1:p.Ala448Val
NM_000102.4:c.1343C>T (CYP17A1) MANE Select	NP_000093.1:p.Ala448Val