Canonical Allele Identifier: CA1525226133
Gene: SRD5A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.6651564A= , CM000667.2:g.6651564A= GRCh38
NC_000005.9:g.6651677A= , CM000667.1:g.6651677A= GRCh37
NC_000005.8:g.6704677A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000504286.2:c.294-278A= ENSP00000518753.1:n.294-278A=
ENST00000510531.6:c.*415-278A= ENSP00000425330.1:n.*415-278A=
ENST00000274192.7:c.294-278A= MANE Select ENSP00000274192.5:n.294-278A=
ENST00000274192.6:c.294-278A= ENSP00000274192.5:n.294-278A=
ENST00000504286.1:n.415-278A=
ENST00000510531.5:c.*415-278A= ENSP00000425330.1:n.*415-278A=
ENST00000513117.1:c.294-4514A= ENSP00000421342.1:n.294-4514A=
NM_001047.2:c.294-278A= NP_001038.1:n.294-278A=
XM_011514103.1:c.320-4514A= XP_011512405.1:n.320-4514A=
NM_001047.3:c.294-278A= NP_001038.1:n.294-278A=
NM_001324322.1:c.320-4514A= NP_001311251.1:n.320-4514A=
NM_001324323.1:c.75-278A= NP_001311252.1:n.75-278A=
NR_136739.1:n.549-278A=
NM_001047.4:c.294-278A= MANE Select NP_001038.1:n.294-278A=
NM_001324322.2:c.320-4514A= NP_001311251.1:n.320-4514A=
NM_001324323.2:c.75-278A= NP_001311252.1:n.75-278A=
NR_136739.2:n.431-278A=