Canonical Allele Identifier: CA377938504

Gene: CYP17A1 WBP1L

Linked Data

• COSMIC: COSM6394179
• MyVariant Identifiers: chr10:g.104591307G>A (hg19) ; chr10:g.102831550G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102831550G>A , CM000672.2:g.102831550G>A	GRCh38
NC_000010.10:g.104591307G>A , CM000672.1:g.104591307G>A	GRCh37
NC_000010.9:g.104581297G>A	NCBI36
NG_007955.1:g.10984C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.1201C>T (CYP17A1) MANE Select	ENSP00000358903.3:p.His401Tyr
ENST00000638190.1:c.898C>T (CYP17A1)	ENSP00000492539.1:p.His300Tyr
ENST00000638272.1:c.745C>T (CYP17A1)	ENSP00000491508.1:p.His249Tyr
ENST00000638971.1:c.1114C>T (CYP17A1)	ENSP00000492313.1:p.His372Tyr
ENST00000639393.1:c.1204C>T (CYP17A1)	ENSP00000492651.1:p.His402Tyr
ENST00000640633.1:n.963C>T (CYP17A1)
ENST00000647664.1:c.*629-48G>A (WBP1L)	ENSP00000498131.1:n.*629-48G>A
ENST00000369887.3:c.1201C>T (CYP17A1)	ENSP00000358903.3:p.His401Tyr
ENST00000469683.1:n.154C>T (CYP17A1)
NM_000102.3:c.1201C>T (CYP17A1)	NP_000093.1:p.His401Tyr
NM_000102.4:c.1201C>T (CYP17A1) MANE Select	NP_000093.1:p.His401Tyr