Canonical Allele Identifier: CA2761730696
Gene: SRD5A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55359711_55359712insAGA , CM000666.2:g.55359711_55359712insAGA GRCh38
NC_000004.11:g.56225878_56225879insAGA , CM000666.1:g.56225878_56225879insAGA GRCh37
NC_000004.10:g.55920635_55920636insAGA NCBI36
NG_028230.1:g.18491_18492insAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000264228.9:c.364+223_364+224insAGA MANE Select ENSP00000264228.4:n.364+223_364+224insAGA
ENST00000677177.2:c.77+223_77+224insAGA
ENST00000678717.1:n.261+223_261+224insAGA
ENST00000679351.1:c.364+223_364+224insAGA ENSP00000505676.1:n.364+223_364+224insAGA
ENST00000679707.1:c.364+223_364+224insAGA ENSP00000505713.1:n.364+223_364+224insAGA
ENST00000679836.1:c.364+223_364+224insAGA ENSP00000506601.1:n.364+223_364+224insAGA
ENST00000680700.1:c.364+223_364+224insAGA ENSP00000504926.1:n.364+223_364+224insAGA
ENST00000264228.8:c.364+223_364+224insAGA ENSP00000264228.4:n.364+223_364+224insAGA
ENST00000505210.1:c.289+223_289+224insAGA ENSP00000424714.1:n.289+223_289+224insAGA
ENST00000514398.1:n.373+223_373+224insAGA
NM_024592.4:c.364+223_364+224insAGA NP_078868.1:n.364+223_364+224insAGA
XM_005265766.2:c.364+223_364+224insAGA XP_005265823.1:n.364+223_364+224insAGA
XM_005265767.2:c.364+223_364+224insAGA XP_005265824.1:n.364+223_364+224insAGA
XM_005265766.4:c.364+223_364+224insAGA XP_005265823.1:n.364+223_364+224insAGA
XM_005265767.3:c.364+223_364+224insAGA XP_005265824.1:n.364+223_364+224insAGA
XM_017008601.1:c.229+223_229+224insAGA XP_016864090.1:n.229+223_229+224insAGA
NM_024592.5:c.364+223_364+224insAGA MANE Select NP_078868.1:n.364+223_364+224insAGA