Canonical Allele Identifier: CA1082265511

Gene: DIAPH1

Linked Data

• dbSNP Id: rs770915828
• gnomAD v3: 5-141524100-C-CAA
• gnomAD v4: 5-141524100-C-CAA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141524101_141524102insAA , CM000667.2:g.141524101_141524102insAA	GRCh38
NC_000005.9:g.140903668_140903669insAA , CM000667.1:g.140903668_140903669insAA	GRCh37
NC_000005.8:g.140883852_140883853insAA	NCBI36
NG_011594.1:g.99955_99956insTT
NG_011594.2:g.99955_99956insTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000389054.8:c.3661+42_3661+43insTT MANE Select	ENSP00000373706.4:n.3661+42_3661+43insTT
ENST00000448451.6:c.67+42_67+43insTT	ENSP00000408159.2:n.67+42_67+43insTT
ENST00000643312.1:c.67+42_67+43insTT	ENSP00000495191.1:n.67+42_67+43insTT
ENST00000643718.1:n.141+42_141+43insTT
ENST00000647433.1:c.3661+42_3661+43insTT	ENSP00000494675.1:n.3661+42_3661+43insTT
ENST00000253811.10:c.3529+42_3529+43insTT	ENSP00000253811.7:n.3529+42_3529+43insTT
ENST00000389054.7:c.3661+42_3661+43insTT	ENSP00000373706.4:n.3661+42_3661+43insTT
ENST00000389057.9:c.3634+42_3634+43insTT	ENSP00000373709.6:n.3634+42_3634+43insTT
ENST00000398557.8:c.3661+42_3661+43insTT	ENSP00000381565.5:n.3661+42_3661+43insTT
ENST00000448451.5:c.197+42_197+43insTT
ENST00000468119.3:n.182+42_182+43insTT
ENST00000476339.1:n.613+42_613+43insTT
ENST00000518047.5:c.3634+42_3634+43insTT	ENSP00000428268.2:n.3634+42_3634+43insTT
NM_001079812.2:c.3634+42_3634+43insTT	NP_001073280.1:n.3634+42_3634+43insTT
NM_001314007.1:c.3661+42_3661+43insTT	NP_001300936.1:n.3661+42_3661+43insTT
NM_005219.4:c.3661+42_3661+43insTT	NP_005210.3:n.3661+42_3661+43insTT
XM_011537572.1:c.3625+42_3625+43insTT	XP_011535874.1:n.3625+42_3625+43insTT
XM_011537573.1:c.3595+42_3595+43insTT	XP_011535875.1:n.3595+42_3595+43insTT
XM_024454384.1:c.3784+42_3784+43insTT	XP_024310152.1:n.3784+42_3784+43insTT
XM_024454385.1:c.3757+42_3757+43insTT	XP_024310153.1:n.3757+42_3757+43insTT
XM_024454386.1:c.3748+42_3748+43insTT	XP_024310154.1:n.3748+42_3748+43insTT
XM_024454387.1:c.3718+42_3718+43insTT	XP_024310155.1:n.3718+42_3718+43insTT
NM_005219.5:c.3661+42_3661+43insTT MANE Select	NP_005210.3:n.3661+42_3661+43insTT
NM_001079812.3:c.3634+42_3634+43insTT	NP_001073280.1:n.3634+42_3634+43insTT
NM_001314007.2:c.3661+42_3661+43insTT	NP_001300936.1:n.3661+42_3661+43insTT