Canonical Allele Identifier: CA2761730563
Gene: SRD5A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55359579_55359584del , CM000666.2:g.55359579_55359584del GRCh38
NC_000004.11:g.56225746_56225751del , CM000666.1:g.56225746_56225751del GRCh37
NC_000004.10:g.55920503_55920508del NCBI36
NG_028230.1:g.18359_18364del

Transcript Alleles

HGVS Amino-acid Change
ENST00000264228.9:c.364+91_364+96del MANE Select ENSP00000264228.4:n.364+91_364+96del
ENST00000677177.2:c.77+91_77+96del
ENST00000678717.1:n.261+91_261+96del
ENST00000679351.1:c.364+91_364+96del ENSP00000505676.1:n.364+91_364+96del
ENST00000679707.1:c.364+91_364+96del ENSP00000505713.1:n.364+91_364+96del
ENST00000679836.1:c.364+91_364+96del ENSP00000506601.1:n.364+91_364+96del
ENST00000680700.1:c.364+91_364+96del ENSP00000504926.1:n.364+91_364+96del
ENST00000264228.8:c.364+91_364+96del ENSP00000264228.4:n.364+91_364+96del
ENST00000505210.1:c.289+91_289+96del ENSP00000424714.1:n.289+91_289+96del
ENST00000514398.1:n.373+91_373+96del
NM_024592.4:c.364+91_364+96del NP_078868.1:n.364+91_364+96del
XM_005265766.2:c.364+91_364+96del XP_005265823.1:n.364+91_364+96del
XM_005265767.2:c.364+91_364+96del XP_005265824.1:n.364+91_364+96del
XM_005265766.4:c.364+91_364+96del XP_005265823.1:n.364+91_364+96del
XM_005265767.3:c.364+91_364+96del XP_005265824.1:n.364+91_364+96del
XM_017008601.1:c.229+91_229+96del XP_016864090.1:n.229+91_229+96del
NM_024592.5:c.364+91_364+96del MANE Select NP_078868.1:n.364+91_364+96del