Canonical Allele Identifier: CA471287163

Gene: CYP17A1 WBP1L

Linked Data

• gnomAD v4: 10-102830852-C-A
• MyVariant Identifiers: chr10:g.104590609C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102830852C>A , CM000672.2:g.102830852C>A	GRCh38
NC_000010.10:g.104590609C>A , CM000672.1:g.104590609C>A	GRCh37
NC_000010.9:g.104580599C>A	NCBI36
NG_007955.1:g.11682G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000369887.4:c.1377G>T (CYP17A1) MANE Select	ENSP00000358903.3:p.Leu459=
ENST00000638190.1:c.1074G>T (CYP17A1)	ENSP00000492539.1:p.Leu358=
ENST00000638272.1:c.921G>T (CYP17A1)	ENSP00000491508.1:p.Leu307=
ENST00000638971.1:c.1290G>T (CYP17A1)	ENSP00000492313.1:p.Leu430=
ENST00000639393.1:c.1380G>T (CYP17A1)	ENSP00000492651.1:p.Leu460=
ENST00000640633.1:n.1139G>T (CYP17A1)
ENST00000647664.1:c.*534C>A (WBP1L)	ENSP00000498131.1:n.*534C>A
ENST00000369887.3:c.1377G>T (CYP17A1)	ENSP00000358903.3:p.Leu459=
NM_000102.3:c.1377G>T (CYP17A1)	NP_000093.1:p.Leu459=
NM_000102.4:c.1377G>T (CYP17A1) MANE Select	NP_000093.1:p.Leu459=