Canonical Allele Identifier: CA1459044792
Gene: SRD5A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55346245C= , CM000666.2:g.55346245C= GRCh38
NC_000004.11:g.56212412C= , CM000666.1:g.56212412C= GRCh37
NC_000004.10:g.55907169C= NCBI36
NG_028230.1:g.5025C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264228.9:c.-92C= MANE Select ENSP00000264228.4:n.-92C=
ENST00000679707.1:c.-92C= ENSP00000505713.1:n.-92C=
ENST00000679836.1:c.-92C= ENSP00000506601.1:n.-92C=
ENST00000264228.8:c.-92C= ENSP00000264228.4:n.-92C=
NM_024592.4:c.-92C= NP_078868.1:n.-92C=
XM_005265766.2:c.-92C= XP_005265823.1:n.-92C=
XM_005265767.2:c.-92C= XP_005265824.1:n.-92C=
XM_005265766.4:c.-92C= XP_005265823.1:n.-92C=
XM_005265767.3:c.-92C= XP_005265824.1:n.-92C=
NM_024592.5:c.-92C= MANE Select NP_078868.1:n.-92C=