Canonical Allele Identifier: CA1459044798
Gene: SRD5A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55346252C= , CM000666.2:g.55346252C= GRCh38
NC_000004.11:g.56212419C= , CM000666.1:g.56212419C= GRCh37
NC_000004.10:g.55907176C= NCBI36
NG_028230.1:g.5032C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264228.9:c.-85C= MANE Select ENSP00000264228.4:n.-85C=
ENST00000679707.1:c.-85C= ENSP00000505713.1:n.-85C=
ENST00000679836.1:c.-85C= ENSP00000506601.1:n.-85C=
ENST00000264228.8:c.-85C= ENSP00000264228.4:n.-85C=
NM_024592.4:c.-85C= NP_078868.1:n.-85C=
XM_005265766.2:c.-85C= XP_005265823.1:n.-85C=
XM_005265767.2:c.-85C= XP_005265824.1:n.-85C=
XM_005265766.4:c.-85C= XP_005265823.1:n.-85C=
XM_005265767.3:c.-85C= XP_005265824.1:n.-85C=
NM_024592.5:c.-85C= MANE Select NP_078868.1:n.-85C=