Canonical Allele Identifier: CA5669345

Gene: CYP17A1 WBP1L

Linked Data

• dbSNP Id: rs769919856
• ExAC: 10:104590704 G / T
• gnomAD v2: 10-104590704-G-T
• gnomAD v4: 10-102830947-G-T
• MyVariant Identifiers: chr10:g.104590704G>T (hg19) ; chr10:g.102830947G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102830947G>T , CM000672.2:g.102830947G>T	GRCh38
NC_000010.10:g.104590704G>T , CM000672.1:g.104590704G>T	GRCh37
NC_000010.9:g.104580694G>T	NCBI36
NG_007955.1:g.11587C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.1282C>A (CYP17A1) MANE Select	ENSP00000358903.3:p.Pro428Thr
ENST00000638190.1:c.979C>A (CYP17A1)	ENSP00000492539.1:p.Pro327Thr
ENST00000638272.1:c.826C>A (CYP17A1)	ENSP00000491508.1:p.Pro276Thr
ENST00000638971.1:c.1195C>A (CYP17A1)	ENSP00000492313.1:p.Pro399Thr
ENST00000639393.1:c.1285C>A (CYP17A1)	ENSP00000492651.1:p.Pro429Thr
ENST00000640633.1:n.1044C>A (CYP17A1)
ENST00000647664.1:c.*628+1G>T (WBP1L)	ENSP00000498131.1:n.*628+1G>T
ENST00000369887.3:c.1282C>A (CYP17A1)	ENSP00000358903.3:p.Pro428Thr
NM_000102.3:c.1282C>A (CYP17A1)	NP_000093.1:p.Pro428Thr
NM_000102.4:c.1282C>A (CYP17A1) MANE Select	NP_000093.1:p.Pro428Thr