Canonical Allele Identifier: CA377938408

Gene: CYP17A1 WBP1L

Linked Data

• MyVariant Identifiers: chr10:g.104591269C>A (hg19) ; chr10:g.102831512C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102831512C>A , CM000672.2:g.102831512C>A	GRCh38
NC_000010.10:g.104591269C>A , CM000672.1:g.104591269C>A	GRCh37
NC_000010.9:g.104581259C>A	NCBI36
NG_007955.1:g.11022G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000369887.4:c.1239G>T (CYP17A1) MANE Select	ENSP00000358903.3:p.Met413Ile
ENST00000638190.1:c.936G>T (CYP17A1)	ENSP00000492539.1:p.Met312Ile
ENST00000638272.1:c.783G>T (CYP17A1)	ENSP00000491508.1:p.Met261Ile
ENST00000638971.1:c.1152G>T (CYP17A1)	ENSP00000492313.1:p.Met384Ile
ENST00000639393.1:c.1242G>T (CYP17A1)	ENSP00000492651.1:p.Met414Ile
ENST00000640633.1:n.1001G>T (CYP17A1)
ENST00000647664.1:c.*629-86C>A (WBP1L)	ENSP00000498131.1:n.*629-86C>A
ENST00000369887.3:c.1239G>T (CYP17A1)	ENSP00000358903.3:p.Met413Ile
ENST00000469683.1:n.192G>T (CYP17A1)
NM_000102.3:c.1239G>T (CYP17A1)	NP_000093.1:p.Met413Ile
NM_000102.4:c.1239G>T (CYP17A1) MANE Select	NP_000093.1:p.Met413Ile