Canonical Allele Identifier: CA1587248342

Gene: DIAPH1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141574049C= , CM000667.2:g.141574049C=	GRCh38
NC_000005.9:g.140953616C= , CM000667.1:g.140953616C=	GRCh37
NC_000005.8:g.140933800C=	NCBI36
NG_011594.1:g.50007G=
NG_011594.2:g.50007G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389054.8:c.1801G= MANE Select	ENSP00000373706.4:p.Ala601=
ENST00000647330.1:c.1778G=	ENSP00000494308.1:n.1778G=
ENST00000647433.1:c.1801G=	ENSP00000494675.1:p.Ala601=
ENST00000253811.10:c.1669G=	ENSP00000253811.7:p.Ala557=
ENST00000389054.7:c.1801G=	ENSP00000373706.4:p.Ala601=
ENST00000389057.9:c.1774G=	ENSP00000373709.6:p.Ala592=
ENST00000398557.8:c.1801G=	ENSP00000381565.5:p.Ala601=
ENST00000518047.5:c.1774G=	ENSP00000428268.2:p.Ala592=
NM_001079812.2:c.1774G=	NP_001073280.1:p.Ala592=
NM_001314007.1:c.1801G=	NP_001300936.1:p.Ala601=
NM_005219.4:c.1801G=	NP_005210.3:p.Ala601=
XM_011537572.1:c.1765G=	XP_011535874.1:p.Ala589=
XM_011537573.1:c.1735G=	XP_011535875.1:p.Ala579=
XM_024454384.1:c.1801G=	XP_024310152.1:p.Ala601=
XM_024454385.1:c.1774G=	XP_024310153.1:p.Ala592=
XM_024454386.1:c.1765G=	XP_024310154.1:p.Ala589=
XM_024454387.1:c.1735G=	XP_024310155.1:p.Ala579=
NM_005219.5:c.1801G= MANE Select	NP_005210.3:p.Ala601=
NM_001079812.3:c.1774G=	NP_001073280.1:p.Ala592=
NM_001314007.2:c.1801G=	NP_001300936.1:p.Ala601=