Canonical Allele Identifier: CA1587248381

Gene: DIAPH1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141574069G= , CM000667.2:g.141574069G=	GRCh38
NC_000005.9:g.140953636G= , CM000667.1:g.140953636G=	GRCh37
NC_000005.8:g.140933820G=	NCBI36
NG_011594.1:g.49987C=
NG_011594.2:g.49987C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389054.8:c.1781C= MANE Select	ENSP00000373706.4:p.Thr594=
ENST00000647330.1:c.1758C=	ENSP00000494308.1:n.1758C=
ENST00000647433.1:c.1781C=	ENSP00000494675.1:p.Thr594=
ENST00000253811.10:c.1649C=	ENSP00000253811.7:p.Thr550=
ENST00000389054.7:c.1781C=	ENSP00000373706.4:p.Thr594=
ENST00000389057.9:c.1754C=	ENSP00000373709.6:p.Thr585=
ENST00000398557.8:c.1781C=	ENSP00000381565.5:p.Thr594=
ENST00000518047.5:c.1754C=	ENSP00000428268.2:p.Thr585=
NM_001079812.2:c.1754C=	NP_001073280.1:p.Thr585=
NM_001314007.1:c.1781C=	NP_001300936.1:p.Thr594=
NM_005219.4:c.1781C=	NP_005210.3:p.Thr594=
XM_011537572.1:c.1745C=	XP_011535874.1:p.Thr582=
XM_011537573.1:c.1715C=	XP_011535875.1:p.Thr572=
XM_024454384.1:c.1781C=	XP_024310152.1:p.Thr594=
XM_024454385.1:c.1754C=	XP_024310153.1:p.Thr585=
XM_024454386.1:c.1745C=	XP_024310154.1:p.Thr582=
XM_024454387.1:c.1715C=	XP_024310155.1:p.Thr572=
NM_005219.5:c.1781C= MANE Select	NP_005210.3:p.Thr594=
NM_001079812.3:c.1754C=	NP_001073280.1:p.Thr585=
NM_001314007.2:c.1781C=	NP_001300936.1:p.Thr594=