Canonical Allele Identifier: CA2574654676
Gene: CYP17A1 HGNC NCBI
WBP1L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102830967del , CM000672.2:g.102830967del GRCh38
NC_000010.10:g.104590724del , CM000672.1:g.104590724del GRCh37
NC_000010.9:g.104580714del NCBI36
NG_007955.1:g.11567del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369887.4:c.1262del (CYP17A1) MANE Select ENSP00000358903.3:p.Ala421GlyfsTer10
ENST00000638190.1:c.959del (CYP17A1) ENSP00000492539.1:p.Ala320GlyfsTer10
ENST00000638272.1:c.806del (CYP17A1) ENSP00000491508.1:p.Ala269GlyfsTer10
ENST00000638971.1:c.1175del (CYP17A1) ENSP00000492313.1:p.Ala392GlyfsTer10
ENST00000639393.1:c.1265del (CYP17A1) ENSP00000492651.1:p.Ala422GlyfsTer10
ENST00000640633.1:n.1024del (CYP17A1)
ENST00000647664.1:c.*628+21del (WBP1L) ENSP00000498131.1:n.*628+21del
ENST00000369887.3:c.1262del (CYP17A1) ENSP00000358903.3:p.Ala421GlyfsTer10
ENST00000469683.1:n.215del (CYP17A1)
NM_000102.3:c.1262del (CYP17A1) NP_000093.1:p.Ala421GlyfsTer10
NM_000102.4:c.1262del (CYP17A1) MANE Select NP_000093.1:p.Ala421GlyfsTer10