Canonical Allele Identifier: CA377937874
Community Standard Title: NM_000102.4(CYP17A1):c.1486C>T (p.Arg496Cys)
Gene: CYP17A1 HGNC NCBI
WBP1L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102830743G>A , CM000672.2:g.102830743G>A GRCh38
NC_000010.10:g.104590500G>A , CM000672.1:g.104590500G>A GRCh37
NC_000010.9:g.104580490G>A NCBI36
NG_007955.1:g.11791C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000102.4:c.1486C>T (CYP17A1) MANE Select NP_000093.1:p.Arg496Cys
ENST00000369887.4:c.1486C>T (CYP17A1) MANE Select ENSP00000358903.3:p.Arg496Cys
NM_000102.3:c.1486C>T (CYP17A1) NP_000093.1:p.Arg496Cys
ENST00000369887.3:c.1486C>T (CYP17A1) ENSP00000358903.3:p.Arg496Cys
ENST00000638190.1:c.1183C>T (CYP17A1) ENSP00000492539.1:p.Arg395Cys
ENST00000638272.1:c.1030C>T (CYP17A1) ENSP00000491508.1:p.Arg344Cys
ENST00000638971.1:c.1399C>T (CYP17A1) ENSP00000492313.1:p.Arg467Cys
ENST00000639393.1:c.1489C>T (CYP17A1) ENSP00000492651.1:p.Arg497Cys
ENST00000640633.1:n.1248C>T (CYP17A1)
ENST00000647664.1:c.*425G>A (WBP1L) ENSP00000498131.1:n.*425G>A