Canonical Allele Identifier: CA3003424145
Gene: CYP17A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102835411dup , CM000672.2:g.102835411dup GRCh38
NC_000010.10:g.104595168dup , CM000672.1:g.104595168dup GRCh37
NC_000010.9:g.104585158dup NCBI36
NG_007955.1:g.7124dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000369887.4:c.298-18dup MANE Select ENSP00000358903.3:n.298-18dup
ENST00000638190.1:c.298-18dup ENSP00000492539.1:n.298-18dup
ENST00000638272.1:c.297+1655dup ENSP00000491508.1:n.297+1655dup
ENST00000638971.1:c.298-18dup ENSP00000492313.1:n.298-18dup
ENST00000639393.1:c.298-18dup ENSP00000492651.1:n.298-18dup
ENST00000640633.1:n.60-18dup
ENST00000369887.3:c.298-18dup ENSP00000358903.3:n.298-18dup
ENST00000489268.1:n.534dup
NM_000102.3:c.298-18dup NP_000093.1:n.298-18dup
NM_000102.4:c.298-18dup MANE Select NP_000093.1:n.298-18dup