Canonical Allele Identifier: CA471288415

Gene: CYP17A1 WBP1L

Linked Data

• MyVariant Identifiers: chr10:g.104592303A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102832546A>C , CM000672.2:g.102832546A>C	GRCh38
NC_000010.10:g.104592303A>C , CM000672.1:g.104592303A>C	GRCh37
NC_000010.9:g.104582293A>C	NCBI36
NG_007955.1:g.9988T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000369887.4:c.1104T>G (CYP17A1) MANE Select	ENSP00000358903.3:p.Pro368=
ENST00000638190.1:c.801T>G (CYP17A1)	ENSP00000492539.1:p.Pro267=
ENST00000638272.1:c.648T>G (CYP17A1)	ENSP00000491508.1:p.Pro216=
ENST00000638971.1:c.1017T>G (CYP17A1)	ENSP00000492313.1:p.Pro339=
ENST00000639393.1:c.1104T>G (CYP17A1)	ENSP00000492651.1:p.Pro368=
ENST00000640633.1:n.866T>G (CYP17A1)
ENST00000647664.1:c.*1577A>C (WBP1L)	ENSP00000498131.1:n.*1577A>C
ENST00000369887.3:c.1104T>G (CYP17A1)	ENSP00000358903.3:p.Pro368=
NM_000102.3:c.1104T>G (CYP17A1)	NP_000093.1:p.Pro368=
NM_000102.4:c.1104T>G (CYP17A1) MANE Select	NP_000093.1:p.Pro368=