Canonical Allele Identifier: CA2675691752
Gene: DIAPH1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.141573855dup , CM000667.2:g.141573855dup GRCh38
NC_000005.9:g.140953422dup , CM000667.1:g.140953422dup GRCh37
NC_000005.8:g.140933606dup NCBI36
NG_011594.1:g.50201dup
NG_011594.2:g.50201dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000389054.8:c.1995dup MANE Select ENSP00000373706.4:p.Pro666ThrfsTer21
ENST00000647433.1:c.1995dup ENSP00000494675.1:p.Pro666ThrfsTer21
ENST00000253811.10:c.1863dup ENSP00000253811.7:p.Pro622ThrfsTer21
ENST00000389054.7:c.1995dup ENSP00000373706.4:p.Pro666ThrfsTer21
ENST00000389057.9:c.1968dup ENSP00000373709.6:p.Pro657ThrfsTer21
ENST00000398557.8:c.1995dup ENSP00000381565.5:p.Pro666ThrfsTer21
ENST00000518047.5:c.1968dup ENSP00000428268.2:p.Pro657ThrfsTer21
NM_001079812.2:c.1968dup NP_001073280.1:p.Pro657ThrfsTer21
NM_001314007.1:c.1995dup NP_001300936.1:p.Pro666ThrfsTer21
NM_005219.4:c.1995dup NP_005210.3:p.Pro666ThrfsTer21
XM_011537572.1:c.1959dup XP_011535874.1:p.Pro654ThrfsTer21
XM_011537573.1:c.1929dup XP_011535875.1:p.Pro644ThrfsTer21
XM_024454384.1:c.1995dup XP_024310152.1:p.Pro666ThrfsTer21
XM_024454385.1:c.1968dup XP_024310153.1:p.Pro657ThrfsTer21
XM_024454386.1:c.1959dup XP_024310154.1:p.Pro654ThrfsTer21
XM_024454387.1:c.1929dup XP_024310155.1:p.Pro644ThrfsTer21
NM_005219.5:c.1995dup MANE Select NP_005210.3:p.Pro666ThrfsTer21
NM_001079812.3:c.1968dup NP_001073280.1:p.Pro657ThrfsTer21
NM_001314007.2:c.1995dup NP_001300936.1:p.Pro666ThrfsTer21