Canonical Allele Identifier: CA1587247651
Gene: DIAPH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.141573824_141573827delinsGGAT , CM000667.2:g.141573824_141573827delinsGGAT GRCh38
NC_000005.9:g.140953391_140953394delinsGGAT , CM000667.1:g.140953391_140953394delinsGGAT GRCh37
NC_000005.8:g.140933575_140933578delinsGGAT NCBI36
NG_011594.1:g.50229_50232delinsATCC
NG_011594.2:g.50229_50232delinsATCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000389054.8:c.2023_2026delinsATCC MANE Select ENSP00000373706.4:p.Ile675=
ENST00000647433.1:c.2023_2026delinsATCC ENSP00000494675.1:p.Ile675=
ENST00000253811.10:c.1891_1894delinsATCC ENSP00000253811.7:p.Ile631=
ENST00000389054.7:c.2023_2026delinsATCC ENSP00000373706.4:p.Ile675=
ENST00000389057.9:c.1996_1999delinsATCC ENSP00000373709.6:p.Ile666=
ENST00000398557.8:c.2023_2026delinsATCC ENSP00000381565.5:p.Ile675=
ENST00000518047.5:c.1996_1999delinsATCC ENSP00000428268.2:p.Ile666=
NM_001079812.2:c.1996_1999delinsATCC NP_001073280.1:p.Ile666=
NM_001314007.1:c.2023_2026delinsATCC NP_001300936.1:p.Ile675=
NM_005219.4:c.2023_2026delinsATCC NP_005210.3:p.Ile675=
XM_011537572.1:c.1987_1990delinsATCC XP_011535874.1:p.Ile663=
XM_011537573.1:c.1957_1960delinsATCC XP_011535875.1:p.Ile653=
XM_024454384.1:c.2023_2026delinsATCC XP_024310152.1:p.Ile675=
XM_024454385.1:c.1996_1999delinsATCC XP_024310153.1:p.Ile666=
XM_024454386.1:c.1987_1990delinsATCC XP_024310154.1:p.Ile663=
XM_024454387.1:c.1957_1960delinsATCC XP_024310155.1:p.Ile653=
NM_005219.5:c.2023_2026delinsATCC MANE Select NP_005210.3:p.Ile675=
NM_001079812.3:c.1996_1999delinsATCC NP_001073280.1:p.Ile666=
NM_001314007.2:c.2023_2026delinsATCC NP_001300936.1:p.Ile675=