Canonical Allele Identifier: CA377939843
Gene: CYP17A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102834841C>A , CM000672.2:g.102834841C>A GRCh38
NC_000010.10:g.104594598C>A , CM000672.1:g.104594598C>A GRCh37
NC_000010.9:g.104584588C>A NCBI36
NG_007955.1:g.7693G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369887.4:c.610G>T MANE Select ENSP00000358903.3:p.Gly204Cys
ENST00000638190.1:c.610G>T ENSP00000492539.1:p.Gly204Cys
ENST00000638272.1:c.298-1633G>T ENSP00000491508.1:n.298-1633G>T
ENST00000638971.1:c.610G>T ENSP00000492313.1:p.Gly204Cys
ENST00000639393.1:c.610G>T ENSP00000492651.1:p.Gly204Cys
ENST00000640633.1:n.372G>T
ENST00000369887.3:c.610G>T ENSP00000358903.3:p.Gly204Cys
ENST00000489268.1:n.864G>T
NM_000102.3:c.610G>T NP_000093.1:p.Gly204Cys
NM_000102.4:c.610G>T MANE Select NP_000093.1:p.Gly204Cys