Canonical Allele Identifier: CA1459044895
Gene: SRD5A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55346376C= , CM000666.2:g.55346376C= GRCh38
NC_000004.11:g.56212543C= , CM000666.1:g.56212543C= GRCh37
NC_000004.10:g.55907300C= NCBI36
NG_028230.1:g.5156C=

Transcript Alleles

HGVS Amino-acid change
ENST00000264228.9:c.40C= MANE Select ENSP00000264228.4:p.Pro14=
ENST00000679351.1:c.40C= ENSP00000505676.1:p.Pro14=
ENST00000679707.1:c.40C= ENSP00000505713.1:p.Pro14=
ENST00000679836.1:c.40C= ENSP00000506601.1:p.Pro14=
ENST00000680700.1:c.40C= ENSP00000504926.1:p.Pro14=
ENST00000264228.8:c.40C= ENSP00000264228.4:p.Pro14=
NM_024592.4:c.40C= NP_078868.1:p.Pro14=
XM_005265766.2:c.40C= XP_005265823.1:p.Pro14=
XM_005265767.2:c.40C= XP_005265824.1:p.Pro14=
XM_005265766.4:c.40C= XP_005265823.1:p.Pro14=
XM_005265767.3:c.40C= XP_005265824.1:p.Pro14=
NM_024592.5:c.40C= MANE Select NP_078868.1:p.Pro14=