Canonical Allele Identifier: CA1153490085

Gene: MASP2 TARDBP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11022212G= , CM000663.2:g.11022212G=	GRCh38
NC_000001.10:g.11082269G= , CM000663.1:g.11082269G=	GRCh37
NC_000001.9:g.11004856G=	NCBI36
NG_008734.1:g.14591G= , LRG_659:g.14591G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700088.1:c.1397-19C= (MASP2)	ENSP00000514787.1:n.1397-19C=
ENST00000240185.8:c.803G= (TARDBP) MANE Select	ENSP00000240185.4:p.Arg268=
ENST00000639083.1:c.803G= (TARDBP)	ENSP00000491203.1:p.Arg268=
ENST00000639599.1:c.803G= (TARDBP)	ENSP00000492196.1:p.Arg268=
ENST00000649624.1:c.768+35G= (TARDBP)	ENSP00000497327.1:n.768+35G=
ENST00000240185.7:c.803G= (TARDBP)	ENSP00000240185.3:p.Arg268=
ENST00000315091.7:c.803G= (TARDBP)	ENSP00000313129.3:p.Arg268=
ENST00000439080.6:c.*384G= (TARDBP)	ENSP00000404666.3:n.*384G=
ENST00000473869.5:c.803G= (TARDBP)	ENSP00000432132.1:p.Arg268=
ENST00000477447.6:c.102G= (TARDBP)
ENST00000610369.4:c.281G= (TARDBP)	ENSP00000482559.1:p.Arg94=
ENST00000611136.4:c.183G=
ENST00000611963.4:c.443G= (TARDBP)	ENSP00000481330.1:p.Arg148=
ENST00000612542.1:c.69G=
ENST00000614494.1:c.221+35G= (TARDBP)
ENST00000614757.4:c.803G=	ENSP00000481867.1:p.Arg268=
ENST00000616545.4:c.803G= (TARDBP)	ENSP00000484722.1:p.Arg268=
ENST00000617172.4:c.544G= (TARDBP)
ENST00000619555.4:c.354G= (TARDBP)
ENST00000620632.4:c.354G= (TARDBP)
ENST00000621715.4:c.632G= (TARDBP)	ENSP00000480690.1:p.Arg211=
ENST00000621790.4:c.803G= (TARDBP)	ENSP00000482191.1:p.Arg268=
ENST00000622057.4:c.550G= (TARDBP)
ENST00000629725.2:c.803G= (TARDBP)	ENSP00000486989.1:p.Arg268=
NM_007375.3:c.803G= , LRG_659t1:c.803G= (TARDBP)	NP_031401.1:p.Arg268=
XR_946596.1:n.925G= (TARDBP)
XR_946597.1:n.925G= (TARDBP)
XM_017000863.2:c.803G= (TARDBP)	XP_016856352.1:p.Arg268=
XM_017000864.2:c.803G= (TARDBP)	XP_016856353.1:p.Arg268=
XM_017000865.2:c.803G= (TARDBP)	XP_016856354.1:p.Arg268=
XM_017000866.2:c.803G= (TARDBP)	XP_016856355.1:p.Arg268=
XM_017000867.2:c.803G= (TARDBP)	XP_016856356.1:p.Arg268=
XM_017000868.2:c.803G= (TARDBP)	XP_016856357.1:p.Arg268=
NM_007375.4:c.803G= (TARDBP) MANE Select	NP_031401.1:p.Arg268=