Canonical Allele Identifier: CA377938281

Gene: CYP17A1 WBP1L

Linked Data

• gnomAD v4: 10-102830934-T-C
• MyVariant Identifiers: chr10:g.104590691T>C (hg19) ; chr10:g.102830934T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102830934T>C , CM000672.2:g.102830934T>C	GRCh38
NC_000010.10:g.104590691T>C , CM000672.1:g.104590691T>C	GRCh37
NC_000010.9:g.104580681T>C	NCBI36
NG_007955.1:g.11600A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.1295A>G (CYP17A1) MANE Select	ENSP00000358903.3:p.Tyr432Cys
ENST00000638190.1:c.992A>G (CYP17A1)	ENSP00000492539.1:p.Tyr331Cys
ENST00000638272.1:c.839A>G (CYP17A1)	ENSP00000491508.1:p.Tyr280Cys
ENST00000638971.1:c.1208A>G (CYP17A1)	ENSP00000492313.1:p.Tyr403Cys
ENST00000639393.1:c.1298A>G (CYP17A1)	ENSP00000492651.1:p.Tyr433Cys
ENST00000640633.1:n.1057A>G (CYP17A1)
ENST00000647664.1:c.*616T>C (WBP1L)	ENSP00000498131.1:n.*616T>C
ENST00000369887.3:c.1295A>G (CYP17A1)	ENSP00000358903.3:p.Tyr432Cys
NM_000102.3:c.1295A>G (CYP17A1)	NP_000093.1:p.Tyr432Cys
NM_000102.4:c.1295A>G (CYP17A1) MANE Select	NP_000093.1:p.Tyr432Cys