Canonical Allele Identifier: CA1153468817

Gene: MASP2 TARDBP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11027317T= , CM000663.2:g.11027317T=	GRCh38
NC_000001.10:g.11087374T= , CM000663.1:g.11087374T=	GRCh37
NC_000001.9:g.11009961T=	NCBI36
NG_007289.1:g.24912A=
NG_008734.1:g.19696T= , LRG_659:g.19696T=
NG_007289.2:g.24912A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699927.1:n.568A= (MASP2)
ENST00000699958.1:c.1524A= (MASP2)	ENSP00000514717.1:p.Val508=
ENST00000700088.1:c.1298-469A= (MASP2)	ENSP00000514787.1:n.1298-469A=
ENST00000700089.1:c.1626A= (MASP2)	ENSP00000514788.1:n.1626A=
ENST00000700090.1:c.1508A= (MASP2)	ENSP00000514789.1:n.1508A=
ENST00000700091.1:c.1431A= (MASP2)	ENSP00000514790.1:p.Val477=
ENST00000700092.1:c.1608A= (MASP2)	ENSP00000514791.1:p.Val536=
ENST00000700093.1:c.1605A= (MASP2)	ENSP00000514792.1:p.Val535=
ENST00000700094.1:c.1637A= (MASP2)	ENSP00000514793.1:n.1637A=
ENST00000700095.1:c.1298-469A= (MASP2)	ENSP00000514794.1:n.1298-469A=
ENST00000700096.1:c.1101-469A= (MASP2)	ENSP00000514795.1:n.1101-469A=
ENST00000700097.1:c.1657A= (MASP2)	ENSP00000514796.1:n.1657A=
ENST00000400897.8:c.1629A= (MASP2) MANE Select	ENSP00000383690.3:p.Val543=
ENST00000400897.7:c.1629A= (MASP2)	ENSP00000383690.3:p.Val543=
ENST00000611136.4:c.448+2109T=
ENST00000612542.1:c.206+2109T=
ENST00000614757.4:c.*452+2109T=	ENSP00000481867.1:n.*452+2109T=
ENST00000620028.1:n.416+2109T=
ENST00000622108.1:c.231+2109T=	ENSP00000480398.1:n.231+2109T=
NM_006610.3:c.1629A= (MASP2)	NP_006601.2:p.Val543=
XM_017000863.2:c.*3011+1652T= (TARDBP)	XP_016856352.1:n.*3011+1652T=
XM_017000864.2:c.*1895+1652T= (TARDBP)	XP_016856353.1:n.*1895+1652T=
XM_017000865.2:c.*1780+2109T= (TARDBP)	XP_016856354.1:n.*1780+2109T=
NM_006610.4:c.1629A= (MASP2) MANE Select	NP_006601.2:p.Val543=