Canonical Allele Identifier: CA377940537
Gene: CYP17A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102835391G>T , CM000672.2:g.102835391G>T GRCh38
NC_000010.10:g.104595148G>T , CM000672.1:g.104595148G>T GRCh37
NC_000010.9:g.104585138G>T NCBI36
NG_007955.1:g.7143C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369887.4:c.299C>A MANE Select ENSP00000358903.3:p.Ala100Glu
ENST00000638190.1:c.299C>A ENSP00000492539.1:p.Ala100Glu
ENST00000638272.1:c.297+1674C>A ENSP00000491508.1:n.297+1674C>A
ENST00000638971.1:c.299C>A ENSP00000492313.1:p.Ala100Glu
ENST00000639393.1:c.299C>A ENSP00000492651.1:p.Ala100Glu
ENST00000640633.1:n.61C>A
ENST00000369887.3:c.299C>A ENSP00000358903.3:p.Ala100Glu
ENST00000489268.1:n.553C>A
NM_000102.3:c.299C>A NP_000093.1:p.Ala100Glu
NM_000102.4:c.299C>A MANE Select NP_000093.1:p.Ala100Glu