Canonical Allele Identifier: CA1932841120
Gene: CYP17A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102837108A= , CM000672.2:g.102837108A= GRCh38
NC_000010.10:g.104596865A= , CM000672.1:g.104596865A= GRCh37
NC_000010.9:g.104586855A= NCBI36
NG_007955.1:g.5426T=

Transcript Alleles

HGVS Amino-acid change
ENST00000369887.4:c.254T= MANE Select ENSP00000358903.3:p.Val85=
ENST00000638190.1:c.254T= ENSP00000492539.1:p.Val85=
ENST00000638272.1:c.254T= ENSP00000491508.1:p.Val85=
ENST00000638971.1:c.254T= ENSP00000492313.1:p.Val85=
ENST00000639393.1:c.254T= ENSP00000492651.1:p.Val85=
ENST00000369887.3:c.254T= ENSP00000358903.3:p.Val85=
ENST00000489268.1:n.307T=
NM_000102.3:c.254T= NP_000093.1:p.Val85=
NM_000102.4:c.254T= MANE Select NP_000093.1:p.Val85=