Canonical Allele Identifier: CA377938696

Gene: CYP17A1 WBP1L

Linked Data

• gnomAD v4: 10-102832530-T-G
• MyVariant Identifiers: chr10:g.104592287T>G (hg19) ; chr10:g.102832530T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102832530T>G , CM000672.2:g.102832530T>G	GRCh38
NC_000010.10:g.104592287T>G , CM000672.1:g.104592287T>G	GRCh37
NC_000010.9:g.104582277T>G	NCBI36
NG_007955.1:g.10004A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000369887.4:c.1120A>C (CYP17A1) MANE Select	ENSP00000358903.3:p.Lys374Gln
ENST00000638190.1:c.817A>C (CYP17A1)	ENSP00000492539.1:p.Lys273Gln
ENST00000638272.1:c.664A>C (CYP17A1)	ENSP00000491508.1:p.Lys222Gln
ENST00000638971.1:c.1033A>C (CYP17A1)	ENSP00000492313.1:p.Lys345Gln
ENST00000639393.1:c.1120A>C (CYP17A1)	ENSP00000492651.1:p.Lys374Gln
ENST00000640633.1:n.882A>C (CYP17A1)
ENST00000647664.1:c.*1561T>G (WBP1L)	ENSP00000498131.1:n.*1561T>G
ENST00000369887.3:c.1120A>C (CYP17A1)	ENSP00000358903.3:p.Lys374Gln
NM_000102.3:c.1120A>C (CYP17A1)	NP_000093.1:p.Lys374Gln
NM_000102.4:c.1120A>C (CYP17A1) MANE Select	NP_000093.1:p.Lys374Gln