Canonical Allele Identifier: CA1459044908
Gene: SRD5A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55346396C= , CM000666.2:g.55346396C= GRCh38
NC_000004.11:g.56212563C= , CM000666.1:g.56212563C= GRCh37
NC_000004.10:g.55907320C= NCBI36
NG_028230.1:g.5176C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264228.9:c.60C= MANE Select ENSP00000264228.4:p.Leu20=
ENST00000679351.1:c.60C= ENSP00000505676.1:p.Leu20=
ENST00000679707.1:c.60C= ENSP00000505713.1:p.Leu20=
ENST00000679836.1:c.60C= ENSP00000506601.1:p.Leu20=
ENST00000680700.1:c.60C= ENSP00000504926.1:p.Leu20=
ENST00000264228.8:c.60C= ENSP00000264228.4:p.Leu20=
NM_024592.4:c.60C= NP_078868.1:p.Leu20=
XM_005265766.2:c.60C= XP_005265823.1:p.Leu20=
XM_005265767.2:c.60C= XP_005265824.1:p.Leu20=
XM_005265766.4:c.60C= XP_005265823.1:p.Leu20=
XM_005265767.3:c.60C= XP_005265824.1:p.Leu20=
NM_024592.5:c.60C= MANE Select NP_078868.1:p.Leu20=