Canonical Allele Identifier: CA2761730517
Gene: SRD5A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55359229_55359230insA , CM000666.2:g.55359229_55359230insA GRCh38
NC_000004.11:g.56225396_56225397insA , CM000666.1:g.56225396_56225397insA GRCh37
NC_000004.10:g.55920153_55920154insA NCBI36
NG_028230.1:g.18009_18010insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000264228.9:c.222-117_222-116insA MANE Select ENSP00000264228.4:n.222-117_222-116insA
ENST00000678717.1:n.119-117_119-116insA
ENST00000679351.1:c.222-117_222-116insA ENSP00000505676.1:n.222-117_222-116insA
ENST00000679707.1:c.222-117_222-116insA ENSP00000505713.1:n.222-117_222-116insA
ENST00000679836.1:c.222-117_222-116insA ENSP00000506601.1:n.222-117_222-116insA
ENST00000680700.1:c.222-117_222-116insA ENSP00000504926.1:n.222-117_222-116insA
ENST00000264228.8:c.222-117_222-116insA ENSP00000264228.4:n.222-117_222-116insA
ENST00000505210.1:c.147-117_147-116insA ENSP00000424714.1:n.147-117_147-116insA
ENST00000514398.1:n.230_230+1insA
NM_024592.4:c.222-117_222-116insA NP_078868.1:n.222-117_222-116insA
XM_005265766.2:c.222-117_222-116insA XP_005265823.1:n.222-117_222-116insA
XM_005265767.2:c.222-117_222-116insA XP_005265824.1:n.222-117_222-116insA
XM_005265766.4:c.222-117_222-116insA XP_005265823.1:n.222-117_222-116insA
XM_005265767.3:c.222-117_222-116insA XP_005265824.1:n.222-117_222-116insA
XM_017008601.1:c.87-117_87-116insA XP_016864090.1:n.87-117_87-116insA
NM_024592.5:c.222-117_222-116insA MANE Select NP_078868.1:n.222-117_222-116insA