Canonical Allele Identifier: CA1587236714

Gene: DIAPH1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141524148C= , CM000667.2:g.141524148C=	GRCh38
NC_000005.9:g.140903715C= , CM000667.1:g.140903715C=	GRCh37
NC_000005.8:g.140883899C=	NCBI36
NG_011594.1:g.99908G=
NG_011594.2:g.99908G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389054.8:c.3656G= MANE Select	ENSP00000373706.4:p.Arg1219=
ENST00000448451.6:c.62G=	ENSP00000408159.2:p.Arg21=
ENST00000643312.1:c.62G=	ENSP00000495191.1:p.Arg21=
ENST00000643718.1:n.136G=
ENST00000647433.1:c.3656G=	ENSP00000494675.1:p.Arg1219=
ENST00000253811.10:c.3524G=	ENSP00000253811.7:p.Arg1175=
ENST00000389054.7:c.3656G=	ENSP00000373706.4:p.Arg1219=
ENST00000389057.9:c.3629G=	ENSP00000373709.6:p.Arg1210=
ENST00000398557.8:c.3656G=	ENSP00000381565.5:p.Arg1219=
ENST00000448451.5:c.192G=
ENST00000468119.3:n.177G=
ENST00000476339.1:n.608G=
ENST00000518047.5:c.3629G=	ENSP00000428268.2:p.Arg1210=
NM_001079812.2:c.3629G=	NP_001073280.1:p.Arg1210=
NM_001314007.1:c.3656G=	NP_001300936.1:p.Arg1219=
NM_005219.4:c.3656G=	NP_005210.3:p.Arg1219=
XM_011537572.1:c.3620G=	XP_011535874.1:p.Arg1207=
XM_011537573.1:c.3590G=	XP_011535875.1:p.Arg1197=
XM_024454384.1:c.3779G=	XP_024310152.1:p.Arg1260=
XM_024454385.1:c.3752G=	XP_024310153.1:p.Arg1251=
XM_024454386.1:c.3743G=	XP_024310154.1:p.Arg1248=
XM_024454387.1:c.3713G=	XP_024310155.1:p.Arg1238=
NM_005219.5:c.3656G= MANE Select	NP_005210.3:p.Arg1219=
NM_001079812.3:c.3629G=	NP_001073280.1:p.Arg1210=
NM_001314007.2:c.3656G=	NP_001300936.1:p.Arg1219=