Canonical Allele Identifier: CA2761730739
Gene: SRD5A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55346276_55346277insA , CM000666.2:g.55346276_55346277insA GRCh38
NC_000004.11:g.56212443_56212444insA , CM000666.1:g.56212443_56212444insA GRCh37
NC_000004.10:g.55907200_55907201insA NCBI36
NG_028230.1:g.5056_5057insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000264228.9:c.-61_-60insA MANE Select ENSP00000264228.4:n.-61_-60insA
ENST00000679707.1:c.-61_-60insA ENSP00000505713.1:n.-61_-60insA
ENST00000679836.1:c.-61_-60insA ENSP00000506601.1:n.-61_-60insA
ENST00000264228.8:c.-61_-60insA ENSP00000264228.4:n.-61_-60insA
NM_024592.4:c.-61_-60insA NP_078868.1:n.-61_-60insA
XM_005265766.2:c.-61_-60insA XP_005265823.1:n.-61_-60insA
XM_005265767.2:c.-61_-60insA XP_005265824.1:n.-61_-60insA
XM_005265766.4:c.-61_-60insA XP_005265823.1:n.-61_-60insA
XM_005265767.3:c.-61_-60insA XP_005265824.1:n.-61_-60insA
NM_024592.5:c.-61_-60insA MANE Select NP_078868.1:n.-61_-60insA