Canonical Allele Identifier: CA356956951
Gene: SRD5A3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55359348A>C , CM000666.2:g.55359348A>C GRCh38
NC_000004.11:g.56225515A>C , CM000666.1:g.56225515A>C GRCh37
NC_000004.10:g.55920272A>C NCBI36
NG_028230.1:g.18128A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264228.9:c.224A>C MANE Select ENSP00000264228.4:p.Tyr75Ser
ENST00000678717.1:n.121A>C
ENST00000679351.1:c.224A>C ENSP00000505676.1:p.Tyr75Ser
ENST00000679707.1:c.224A>C ENSP00000505713.1:p.Tyr75Ser
ENST00000679836.1:c.224A>C ENSP00000506601.1:p.Tyr75Ser
ENST00000680700.1:c.224A>C ENSP00000504926.1:p.Tyr75Ser
ENST00000264228.8:c.224A>C ENSP00000264228.4:p.Tyr75Ser
ENST00000505210.1:c.149A>C ENSP00000424714.1:p.Tyr50Ser
ENST00000514398.1:n.233A>C
NM_024592.4:c.224A>C NP_078868.1:p.Tyr75Ser
XM_005265766.2:c.224A>C XP_005265823.1:p.Tyr75Ser
XM_005265767.2:c.224A>C XP_005265824.1:p.Tyr75Ser
XM_005265766.4:c.224A>C XP_005265823.1:p.Tyr75Ser
XM_005265767.3:c.224A>C XP_005265824.1:p.Tyr75Ser
XM_017008601.1:c.89A>C XP_016864090.1:p.Tyr30Ser
NM_024592.5:c.224A>C MANE Select NP_078868.1:p.Tyr75Ser