Canonical Allele Identifier: CA1587247879
Gene: DIAPH1 HGNC NCBI

Linked Data

dbSNP Id: rs2099895569

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.141573913_141573916del , CM000667.2:g.141573913_141573916del GRCh38
NC_000005.9:g.140953480_140953483del , CM000667.1:g.140953480_140953483del GRCh37
NC_000005.8:g.140933664_140933667del NCBI36
NG_011594.1:g.50142_50145del
NG_011594.2:g.50142_50145del

Transcript Alleles

HGVS Amino-acid Change
ENST00000389054.8:c.1936_1939del MANE Select ENSP00000373706.4:p.Ser646GlyfsTer?
ENST00000647433.1:c.1936_1939del ENSP00000494675.1:p.Ser646GlyfsTer?
ENST00000253811.10:c.1804_1807del ENSP00000253811.7:p.Ser602GlyfsTer?
ENST00000389054.7:c.1936_1939del ENSP00000373706.4:p.Ser646GlyfsTer?
ENST00000389057.9:c.1909_1912del ENSP00000373709.6:p.Ser637GlyfsTer?
ENST00000398557.8:c.1936_1939del ENSP00000381565.5:p.Ser646GlyfsTer?
ENST00000518047.5:c.1909_1912del ENSP00000428268.2:p.Ser637GlyfsTer?
NM_001079812.2:c.1909_1912del NP_001073280.1:p.Ser637GlyfsTer?
NM_001314007.1:c.1936_1939del NP_001300936.1:p.Ser646GlyfsTer?
NM_005219.4:c.1936_1939del NP_005210.3:p.Ser646GlyfsTer?
XM_011537572.1:c.1900_1903del XP_011535874.1:p.Ser634GlyfsTer?
XM_011537573.1:c.1870_1873del XP_011535875.1:p.Ser624GlyfsTer?
XM_024454384.1:c.1936_1939del XP_024310152.1:p.Ser646GlyfsTer?
XM_024454385.1:c.1909_1912del XP_024310153.1:p.Ser637GlyfsTer?
XM_024454386.1:c.1900_1903del XP_024310154.1:p.Ser634GlyfsTer?
XM_024454387.1:c.1870_1873del XP_024310155.1:p.Ser624GlyfsTer?
NM_005219.5:c.1936_1939del MANE Select NP_005210.3:p.Ser646GlyfsTer?
NM_001079812.3:c.1909_1912del NP_001073280.1:p.Ser637GlyfsTer?
NM_001314007.2:c.1936_1939del NP_001300936.1:p.Ser646GlyfsTer?