Canonical Allele Identifier: CA377937989

Gene: CYP17A1 WBP1L

Linked Data

• dbSNP Id: rs1242989937
• gnomAD v2: 10-104590553-C-T
• gnomAD v4: 10-102830796-C-T
• MyVariant Identifiers: chr10:g.104590553C>T (hg19) ; chr10:g.102830796C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102830796C>T , CM000672.2:g.102830796C>T	GRCh38
NC_000010.10:g.104590553C>T , CM000672.1:g.104590553C>T	GRCh37
NC_000010.9:g.104580543C>T	NCBI36
NG_007955.1:g.11738G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.1433G>A (CYP17A1) MANE Select	ENSP00000358903.3:p.Gly478Asp
ENST00000638190.1:c.1130G>A (CYP17A1)	ENSP00000492539.1:p.Gly377Asp
ENST00000638272.1:c.977G>A (CYP17A1)	ENSP00000491508.1:p.Gly326Asp
ENST00000638971.1:c.1346G>A (CYP17A1)	ENSP00000492313.1:p.Gly449Asp
ENST00000639393.1:c.1436G>A (CYP17A1)	ENSP00000492651.1:p.Gly479Asp
ENST00000640633.1:n.1195G>A (CYP17A1)
ENST00000647664.1:c.*478C>T (WBP1L)	ENSP00000498131.1:n.*478C>T
ENST00000369887.3:c.1433G>A (CYP17A1)	ENSP00000358903.3:p.Gly478Asp
NM_000102.3:c.1433G>A (CYP17A1)	NP_000093.1:p.Gly478Asp
NM_000102.4:c.1433G>A (CYP17A1) MANE Select	NP_000093.1:p.Gly478Asp