Canonical Allele Identifier: CA356956963
Gene: SRD5A3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55359352T>A , CM000666.2:g.55359352T>A GRCh38
NC_000004.11:g.56225519T>A , CM000666.1:g.56225519T>A GRCh37
NC_000004.10:g.55920276T>A NCBI36
NG_028230.1:g.18132T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264228.9:c.228T>A MANE Select ENSP00000264228.4:p.Phe76Leu
ENST00000678717.1:n.125T>A
ENST00000679351.1:c.228T>A ENSP00000505676.1:p.Phe76Leu
ENST00000679707.1:c.228T>A ENSP00000505713.1:p.Phe76Leu
ENST00000679836.1:c.228T>A ENSP00000506601.1:p.Phe76Leu
ENST00000680700.1:c.228T>A ENSP00000504926.1:p.Phe76Leu
ENST00000264228.8:c.228T>A ENSP00000264228.4:p.Phe76Leu
ENST00000505210.1:c.153T>A ENSP00000424714.1:p.Phe51Leu
ENST00000514398.1:n.237T>A
NM_024592.4:c.228T>A NP_078868.1:p.Phe76Leu
XM_005265766.2:c.228T>A XP_005265823.1:p.Phe76Leu
XM_005265767.2:c.228T>A XP_005265824.1:p.Phe76Leu
XM_005265766.4:c.228T>A XP_005265823.1:p.Phe76Leu
XM_005265767.3:c.228T>A XP_005265824.1:p.Phe76Leu
XM_017008601.1:c.93T>A XP_016864090.1:p.Phe31Leu
NM_024592.5:c.228T>A MANE Select NP_078868.1:p.Phe76Leu