Canonical Allele Identifier: CA2670675020
Gene: SRD5A3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55359154_55359155del , CM000666.2:g.55359154_55359155del GRCh38
NC_000004.11:g.56225321_56225322del , CM000666.1:g.56225321_56225322del GRCh37
NC_000004.10:g.55920078_55920079del NCBI36
NG_028230.1:g.17934_17935del

Transcript Alleles

HGVS Amino-acid Change
ENST00000264228.9:c.222-192_222-191del MANE Select ENSP00000264228.4:n.222-192_222-191del
ENST00000678717.1:n.119-192_119-191del
ENST00000679351.1:c.222-192_222-191del ENSP00000505676.1:n.222-192_222-191del
ENST00000679707.1:c.222-192_222-191del ENSP00000505713.1:n.222-192_222-191del
ENST00000679836.1:c.222-192_222-191del ENSP00000506601.1:n.222-192_222-191del
ENST00000680700.1:c.222-192_222-191del ENSP00000504926.1:n.222-192_222-191del
ENST00000264228.8:c.222-192_222-191del ENSP00000264228.4:n.222-192_222-191del
ENST00000505210.1:c.147-192_147-191del ENSP00000424714.1:n.147-192_147-191del
ENST00000514398.1:n.155_156del
NM_024592.4:c.222-192_222-191del NP_078868.1:n.222-192_222-191del
XM_005265766.2:c.222-192_222-191del XP_005265823.1:n.222-192_222-191del
XM_005265767.2:c.222-192_222-191del XP_005265824.1:n.222-192_222-191del
XM_005265766.4:c.222-192_222-191del XP_005265823.1:n.222-192_222-191del
XM_005265767.3:c.222-192_222-191del XP_005265824.1:n.222-192_222-191del
XM_017008601.1:c.87-192_87-191del XP_016864090.1:n.87-192_87-191del
NM_024592.5:c.222-192_222-191del MANE Select NP_078868.1:n.222-192_222-191del