Canonical Allele Identifier: CA471287164

Gene: CYP17A1 WBP1L

Linked Data

• dbSNP Id: rs1298828236
• gnomAD v2: 10-104590611-G-A
• gnomAD v4: 10-102830854-G-A
• MyVariant Identifiers: chr10:g.104590611G>A (hg19) ; chr10:g.102830854G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102830854G>A , CM000672.2:g.102830854G>A	GRCh38
NC_000010.10:g.104590611G>A , CM000672.1:g.104590611G>A	GRCh37
NC_000010.9:g.104580601G>A	NCBI36
NG_007955.1:g.11680C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000369887.4:c.1375C>T (CYP17A1) MANE Select	ENSP00000358903.3:p.Leu459=
ENST00000638190.1:c.1072C>T (CYP17A1)	ENSP00000492539.1:p.Leu358=
ENST00000638272.1:c.919C>T (CYP17A1)	ENSP00000491508.1:p.Leu307=
ENST00000638971.1:c.1288C>T (CYP17A1)	ENSP00000492313.1:p.Leu430=
ENST00000639393.1:c.1378C>T (CYP17A1)	ENSP00000492651.1:p.Leu460=
ENST00000640633.1:n.1137C>T (CYP17A1)
ENST00000647664.1:c.*536G>A (WBP1L)	ENSP00000498131.1:n.*536G>A
ENST00000369887.3:c.1375C>T (CYP17A1)	ENSP00000358903.3:p.Leu459=
NM_000102.3:c.1375C>T (CYP17A1)	NP_000093.1:p.Leu459=
NM_000102.4:c.1375C>T (CYP17A1) MANE Select	NP_000093.1:p.Leu459=