Canonical Allele Identifier: CA645558435

Gene: DIAPH1

Linked Data

• COSMIC: COSM6441337

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141573919_141573920delinsAA , CM000667.2:g.141573919_141573920delinsAA	GRCh38
NC_000005.9:g.140953486_140953487delinsAA , CM000667.1:g.140953486_140953487delinsAA	GRCh37
NC_000005.8:g.140933670_140933671delinsAA	NCBI36
NG_011594.1:g.50136_50137delinsTT
NG_011594.2:g.50136_50137delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389054.8:c.1930_1931delinsTT MANE Select	ENSP00000373706.4:p.Pro644Phe
ENST00000647433.1:c.1930_1931delinsTT	ENSP00000494675.1:p.Pro644Phe
ENST00000253811.10:c.1798_1799delinsTT	ENSP00000253811.7:p.Pro600Phe
ENST00000389054.7:c.1930_1931delinsTT	ENSP00000373706.4:p.Pro644Phe
ENST00000389057.9:c.1903_1904delinsTT	ENSP00000373709.6:p.Pro635Phe
ENST00000398557.8:c.1930_1931delinsTT	ENSP00000381565.5:p.Pro644Phe
ENST00000518047.5:c.1903_1904delinsTT	ENSP00000428268.2:p.Pro635Phe
NM_001079812.2:c.1903_1904delinsTT	NP_001073280.1:p.Pro635Phe
NM_001314007.1:c.1930_1931delinsTT	NP_001300936.1:p.Pro644Phe
NM_005219.4:c.1930_1931delinsTT	NP_005210.3:p.Pro644Phe
XM_011537572.1:c.1894_1895delinsTT	XP_011535874.1:p.Pro632Phe
XM_011537573.1:c.1864_1865delinsTT	XP_011535875.1:p.Pro622Phe
XM_024454384.1:c.1930_1931delinsTT	XP_024310152.1:p.Pro644Phe
XM_024454385.1:c.1903_1904delinsTT	XP_024310153.1:p.Pro635Phe
XM_024454386.1:c.1894_1895delinsTT	XP_024310154.1:p.Pro632Phe
XM_024454387.1:c.1864_1865delinsTT	XP_024310155.1:p.Pro622Phe
NM_005219.5:c.1930_1931delinsTT MANE Select	NP_005210.3:p.Pro644Phe
NM_001079812.3:c.1903_1904delinsTT	NP_001073280.1:p.Pro635Phe
NM_001314007.2:c.1930_1931delinsTT	NP_001300936.1:p.Pro644Phe