Canonical Allele Identifier: CA377938465

Gene: CYP17A1 WBP1L

Linked Data

• ClinVar Variation Id: 2585193
• ClinVar RCV Id: RCV003337809
• dbSNP Id: rs104894143
• MyVariant Identifiers: chr10:g.104591292A>C (hg19) ; chr10:g.102831535A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102831535A>C , CM000672.2:g.102831535A>C	GRCh38
NC_000010.10:g.104591292A>C , CM000672.1:g.104591292A>C	GRCh37
NC_000010.9:g.104581282A>C	NCBI36
NG_007955.1:g.10999T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000369887.4:c.1216T>G (CYP17A1) MANE Select	ENSP00000358903.3:p.Trp406Gly
ENST00000638190.1:c.913T>G (CYP17A1)	ENSP00000492539.1:p.Trp305Gly
ENST00000638272.1:c.760T>G (CYP17A1)	ENSP00000491508.1:p.Trp254Gly
ENST00000638971.1:c.1129T>G (CYP17A1)	ENSP00000492313.1:p.Trp377Gly
ENST00000639393.1:c.1219T>G (CYP17A1)	ENSP00000492651.1:p.Trp407Gly
ENST00000640633.1:n.978T>G (CYP17A1)
ENST00000647664.1:c.*629-63A>C (WBP1L)	ENSP00000498131.1:n.*629-63A>C
ENST00000369887.3:c.1216T>G (CYP17A1)	ENSP00000358903.3:p.Trp406Gly
ENST00000469683.1:n.169T>G (CYP17A1)
NM_000102.3:c.1216T>G (CYP17A1)	NP_000093.1:p.Trp406Gly
NM_000102.4:c.1216T>G (CYP17A1) MANE Select	NP_000093.1:p.Trp406Gly