Canonical Allele Identifier: CA471287461

Gene: CYP17A1 WBP1L

Linked Data

• gnomAD v4: 10-102830966-C-G
• MyVariant Identifiers: chr10:g.104590723C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102830966C>G , CM000672.2:g.102830966C>G	GRCh38
NC_000010.10:g.104590723C>G , CM000672.1:g.104590723C>G	GRCh37
NC_000010.9:g.104580713C>G	NCBI36
NG_007955.1:g.11568G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.1263G>C (CYP17A1) MANE Select	ENSP00000358903.3:p.Ala421=
ENST00000638190.1:c.960G>C (CYP17A1)	ENSP00000492539.1:p.Ala320=
ENST00000638272.1:c.807G>C (CYP17A1)	ENSP00000491508.1:p.Ala269=
ENST00000638971.1:c.1176G>C (CYP17A1)	ENSP00000492313.1:p.Ala392=
ENST00000639393.1:c.1266G>C (CYP17A1)	ENSP00000492651.1:p.Ala422=
ENST00000640633.1:n.1025G>C (CYP17A1)
ENST00000647664.1:c.*628+20C>G (WBP1L)	ENSP00000498131.1:n.*628+20C>G
ENST00000369887.3:c.1263G>C (CYP17A1)	ENSP00000358903.3:p.Ala421=
ENST00000469683.1:n.216G>C (CYP17A1)
NM_000102.3:c.1263G>C (CYP17A1)	NP_000093.1:p.Ala421=
NM_000102.4:c.1263G>C (CYP17A1) MANE Select	NP_000093.1:p.Ala421=