Canonical Allele Identifier: CA2578275994
Gene: SRD5A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.6651760A>T , CM000667.2:g.6651760A>T GRCh38
NC_000005.9:g.6651873A>T , CM000667.1:g.6651873A>T GRCh37
NC_000005.8:g.6704873A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000504286.2:c.294-82A>T ENSP00000518753.1:n.294-82A>T
ENST00000510531.6:c.*415-82A>T ENSP00000425330.1:n.*415-82A>T
ENST00000274192.7:c.294-82A>T MANE Select ENSP00000274192.5:n.294-82A>T
ENST00000274192.6:c.294-82A>T ENSP00000274192.5:n.294-82A>T
ENST00000504286.1:n.415-82A>T
ENST00000510531.5:c.*415-82A>T ENSP00000425330.1:n.*415-82A>T
ENST00000513117.1:c.294-4318A>T ENSP00000421342.1:n.294-4318A>T
NM_001047.2:c.294-82A>T NP_001038.1:n.294-82A>T
XM_011514103.1:c.320-4318A>T XP_011512405.1:n.320-4318A>T
NM_001047.3:c.294-82A>T NP_001038.1:n.294-82A>T
NM_001324322.1:c.320-4318A>T NP_001311251.1:n.320-4318A>T
NM_001324323.1:c.75-82A>T NP_001311252.1:n.75-82A>T
NR_136739.1:n.549-82A>T
NM_001047.4:c.294-82A>T MANE Select NP_001038.1:n.294-82A>T
NM_001324322.2:c.320-4318A>T NP_001311251.1:n.320-4318A>T
NM_001324323.2:c.75-82A>T NP_001311252.1:n.75-82A>T
NR_136739.2:n.431-82A>T