Canonical Allele Identifier: CA1459044888
Gene: SRD5A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55346365_55346366delinsCG , CM000666.2:g.55346365_55346366delinsCG GRCh38
NC_000004.11:g.56212532_56212533delinsCG , CM000666.1:g.56212532_56212533delinsCG GRCh37
NC_000004.10:g.55907289_55907290delinsCG NCBI36
NG_028230.1:g.5145_5146delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000264228.9:c.29_30delinsCG MANE Select ENSP00000264228.4:p.Ser10=
ENST00000679351.1:c.29_30delinsCG ENSP00000505676.1:p.Ser10=
ENST00000679707.1:c.29_30delinsCG ENSP00000505713.1:p.Ser10=
ENST00000679836.1:c.29_30delinsCG ENSP00000506601.1:p.Ser10=
ENST00000680700.1:c.29_30delinsCG ENSP00000504926.1:p.Ser10=
ENST00000264228.8:c.29_30delinsCG ENSP00000264228.4:p.Ser10=
NM_024592.4:c.29_30delinsCG NP_078868.1:p.Ser10=
XM_005265766.2:c.29_30delinsCG XP_005265823.1:p.Ser10=
XM_005265767.2:c.29_30delinsCG XP_005265824.1:p.Ser10=
XM_005265766.4:c.29_30delinsCG XP_005265823.1:p.Ser10=
XM_005265767.3:c.29_30delinsCG XP_005265824.1:p.Ser10=
NM_024592.5:c.29_30delinsCG MANE Select NP_078868.1:p.Ser10=