Canonical Allele Identifier: CA356957078
Gene: SRD5A3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55359404C>T , CM000666.2:g.55359404C>T GRCh38
NC_000004.11:g.56225571C>T , CM000666.1:g.56225571C>T GRCh37
NC_000004.10:g.55920328C>T NCBI36
NG_028230.1:g.18184C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264228.9:c.280C>T MANE Select ENSP00000264228.4:p.Leu94Phe
ENST00000678717.1:n.177C>T
ENST00000679351.1:c.280C>T ENSP00000505676.1:p.Leu94Phe
ENST00000679707.1:c.280C>T ENSP00000505713.1:p.Leu94Phe
ENST00000679836.1:c.280C>T ENSP00000506601.1:p.Leu94Phe
ENST00000680700.1:c.280C>T ENSP00000504926.1:p.Leu94Phe
ENST00000264228.8:c.280C>T ENSP00000264228.4:p.Leu94Phe
ENST00000505210.1:c.205C>T ENSP00000424714.1:p.Leu69Phe
ENST00000514398.1:n.289C>T
NM_024592.4:c.280C>T NP_078868.1:p.Leu94Phe
XM_005265766.2:c.280C>T XP_005265823.1:p.Leu94Phe
XM_005265767.2:c.280C>T XP_005265824.1:p.Leu94Phe
XM_005265766.4:c.280C>T XP_005265823.1:p.Leu94Phe
XM_005265767.3:c.280C>T XP_005265824.1:p.Leu94Phe
XM_017008601.1:c.145C>T XP_016864090.1:p.Leu49Phe
NM_024592.5:c.280C>T MANE Select NP_078868.1:p.Leu94Phe