Canonical Allele Identifier: CA1587228691
Gene: DIAPH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.141515046T= , CM000667.2:g.141515046T= GRCh38
NC_000005.9:g.140894613T= , CM000667.1:g.140894613T= GRCh37
NC_000005.8:g.140874797T= NCBI36
NG_011594.1:g.109010A=
NG_011594.2:g.109010A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000389054.8:c.*1805A= MANE Select ENSP00000373706.4:n.*1805A=
ENST00000647433.1:c.*1924A= ENSP00000494675.1:n.*1924A=
ENST00000253811.10:c.*1805A= ENSP00000253811.7:n.*1805A=
ENST00000389054.7:c.*1805A= ENSP00000373706.4:n.*1805A=
ENST00000389057.9:c.*1805A= ENSP00000373709.6:n.*1805A=
ENST00000398557.8:c.*1805A= ENSP00000381565.5:n.*1805A=
ENST00000476339.1:n.2576A=
NM_001079812.2:c.*1805A= NP_001073280.1:n.*1805A=
NM_001314007.1:c.*1924A= NP_001300936.1:n.*1924A=
NM_005219.4:c.*1805A= NP_005210.3:n.*1805A=
XM_011537572.1:c.*1805A= XP_011535874.1:n.*1805A=
XM_011537573.1:c.*1805A= XP_011535875.1:n.*1805A=
XM_024454384.1:c.*1805A= XP_024310152.1:n.*1805A=
XM_024454385.1:c.*1805A= XP_024310153.1:n.*1805A=
XM_024454386.1:c.*1805A= XP_024310154.1:n.*1805A=
XM_024454387.1:c.*1805A= XP_024310155.1:n.*1805A=
NM_005219.5:c.*1805A= MANE Select NP_005210.3:n.*1805A=
NM_001079812.3:c.*1805A= NP_001073280.1:n.*1805A=
NM_001314007.2:c.*1924A= NP_001300936.1:n.*1924A=