Canonical Allele Identifier: CA2761730735
Gene: SRD5A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55346271_55346272insAGA , CM000666.2:g.55346271_55346272insAGA GRCh38
NC_000004.11:g.56212438_56212439insAGA , CM000666.1:g.56212438_56212439insAGA GRCh37
NC_000004.10:g.55907195_55907196insAGA NCBI36
NG_028230.1:g.5051_5052insAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000264228.9:c.-66_-65insAGA MANE Select ENSP00000264228.4:n.-66_-65insAGA
ENST00000679707.1:c.-66_-65insAGA ENSP00000505713.1:n.-66_-65insAGA
ENST00000679836.1:c.-66_-65insAGA ENSP00000506601.1:n.-66_-65insAGA
ENST00000264228.8:c.-66_-65insAGA ENSP00000264228.4:n.-66_-65insAGA
NM_024592.4:c.-66_-65insAGA NP_078868.1:n.-66_-65insAGA
XM_005265766.2:c.-66_-65insAGA XP_005265823.1:n.-66_-65insAGA
XM_005265767.2:c.-66_-65insAGA XP_005265824.1:n.-66_-65insAGA
XM_005265766.4:c.-66_-65insAGA XP_005265823.1:n.-66_-65insAGA
XM_005265767.3:c.-66_-65insAGA XP_005265824.1:n.-66_-65insAGA
NM_024592.5:c.-66_-65insAGA MANE Select NP_078868.1:n.-66_-65insAGA