Canonical Allele Identifier: CA1553916196

Gene: MARVELD2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.69419790_69419791delinsTC , CM000667.2:g.69419790_69419791delinsTC	GRCh38
NC_000005.9:g.68715617_68715618delinsTC , CM000667.1:g.68715617_68715618delinsTC	GRCh37
NC_000005.8:g.68751373_68751374delinsTC	NCBI36
NG_017201.1:g.9679_9680delinsTC
NG_017201.2:g.9679_9680delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325631.10:c.405_406delinsTC MANE Select	ENSP00000323264.5:p.Asp135=
ENST00000413223.3:c.405_406delinsTC	ENSP00000398922.2:p.Asp135=
ENST00000436532.7:c.405_406delinsTC	ENSP00000414776.2:p.Asp135=
ENST00000645446.1:c.405_406delinsTC	ENSP00000494616.1:p.Asp135=
ENST00000647531.1:c.405_406delinsTC	ENSP00000493858.1:p.Asp135=
ENST00000325631.9:c.405_406delinsTC	ENSP00000323264.5:p.Asp135=
ENST00000413223.2:c.405_406delinsTC	ENSP00000398922.2:p.Asp135=
ENST00000436532.6:c.405_406delinsTC	ENSP00000414776.2:p.Asp135=
ENST00000454295.6:c.405_406delinsTC	ENSP00000396244.2:p.Asp135=
ENST00000512803.5:c.405_406delinsTC	ENSP00000423490.1:p.Asp135=
ENST00000515844.1:c.405_406delinsTC	ENSP00000421902.1:p.Asp135=
NM_001038603.2:c.405_406delinsTC	NP_001033692.2:p.Asp135=
NM_001244734.1:c.405_406delinsTC	NP_001231663.1:p.Asp135=
XM_005248445.3:c.405_406delinsTC	XP_005248502.1:p.Asp135=
XM_005248446.3:c.405_406delinsTC	XP_005248503.1:p.Asp135=
XM_005248447.3:c.405_406delinsTC	XP_005248504.1:p.Asp135=
XM_005248445.4:c.405_406delinsTC	XP_005248502.1:p.Asp135=
XM_005248446.4:c.405_406delinsTC	XP_005248503.1:p.Asp135=
XM_005248447.4:c.405_406delinsTC	XP_005248504.1:p.Asp135=
NM_001038603.3:c.405_406delinsTC MANE Select	NP_001033692.2:p.Asp135=
NM_001244734.2:c.405_406delinsTC	NP_001231663.1:p.Asp135=