Canonical Allele Identifier: CA1587236615

Gene: DIAPH1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141524101_141524102delinsAC , CM000667.2:g.141524101_141524102delinsAC	GRCh38
NC_000005.9:g.140903668_140903669delinsAC , CM000667.1:g.140903668_140903669delinsAC	GRCh37
NC_000005.8:g.140883852_140883853delinsAC	NCBI36
NG_011594.1:g.99954_99955delinsGT
NG_011594.2:g.99954_99955delinsGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000389054.8:c.3661+41_3661+42delinsGT MANE Select	ENSP00000373706.4:n.3661+41_3661+42delinsGT
ENST00000448451.6:c.67+41_67+42delinsGT	ENSP00000408159.2:n.67+41_67+42delinsGT
ENST00000643312.1:c.67+41_67+42delinsGT	ENSP00000495191.1:n.67+41_67+42delinsGT
ENST00000643718.1:n.141+41_141+42delinsGT
ENST00000647433.1:c.3661+41_3661+42delinsGT	ENSP00000494675.1:n.3661+41_3661+42delinsGT
ENST00000253811.10:c.3529+41_3529+42delinsGT	ENSP00000253811.7:n.3529+41_3529+42delinsGT
ENST00000389054.7:c.3661+41_3661+42delinsGT	ENSP00000373706.4:n.3661+41_3661+42delinsGT
ENST00000389057.9:c.3634+41_3634+42delinsGT	ENSP00000373709.6:n.3634+41_3634+42delinsGT
ENST00000398557.8:c.3661+41_3661+42delinsGT	ENSP00000381565.5:n.3661+41_3661+42delinsGT
ENST00000448451.5:c.197+41_197+42delinsGT
ENST00000468119.3:n.182+41_182+42delinsGT
ENST00000476339.1:n.613+41_613+42delinsGT
ENST00000518047.5:c.3634+41_3634+42delinsGT	ENSP00000428268.2:n.3634+41_3634+42delinsGT
NM_001079812.2:c.3634+41_3634+42delinsGT	NP_001073280.1:n.3634+41_3634+42delinsGT
NM_001314007.1:c.3661+41_3661+42delinsGT	NP_001300936.1:n.3661+41_3661+42delinsGT
NM_005219.4:c.3661+41_3661+42delinsGT	NP_005210.3:n.3661+41_3661+42delinsGT
XM_011537572.1:c.3625+41_3625+42delinsGT	XP_011535874.1:n.3625+41_3625+42delinsGT
XM_011537573.1:c.3595+41_3595+42delinsGT	XP_011535875.1:n.3595+41_3595+42delinsGT
XM_024454384.1:c.3784+41_3784+42delinsGT	XP_024310152.1:n.3784+41_3784+42delinsGT
XM_024454385.1:c.3757+41_3757+42delinsGT	XP_024310153.1:n.3757+41_3757+42delinsGT
XM_024454386.1:c.3748+41_3748+42delinsGT	XP_024310154.1:n.3748+41_3748+42delinsGT
XM_024454387.1:c.3718+41_3718+42delinsGT	XP_024310155.1:n.3718+41_3718+42delinsGT
NM_005219.5:c.3661+41_3661+42delinsGT MANE Select	NP_005210.3:n.3661+41_3661+42delinsGT
NM_001079812.3:c.3634+41_3634+42delinsGT	NP_001073280.1:n.3634+41_3634+42delinsGT
NM_001314007.2:c.3661+41_3661+42delinsGT	NP_001300936.1:n.3661+41_3661+42delinsGT