Canonical Allele Identifier: CA1153469021

Gene: MASP2 TARDBP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11027465G= , CM000663.2:g.11027465G=	GRCh38
NC_000001.10:g.11087522G= , CM000663.1:g.11087522G=	GRCh37
NC_000001.9:g.11010109G=	NCBI36
NG_007289.1:g.24764C=
NG_008734.1:g.19844G= , LRG_659:g.19844G=
NG_007289.2:g.24764C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699927.1:n.420C= (MASP2)
ENST00000699958.1:c.1376C= (MASP2)	ENSP00000514717.1:p.Ala459=
ENST00000700088.1:c.1298-617C= (MASP2)	ENSP00000514787.1:n.1298-617C=
ENST00000700089.1:c.1478C= (MASP2)	ENSP00000514788.1:n.1478C=
ENST00000700090.1:c.1360C= (MASP2)	ENSP00000514789.1:n.1360C=
ENST00000700091.1:c.1283C= (MASP2)	ENSP00000514790.1:p.Ala428=
ENST00000700092.1:c.1460C= (MASP2)	ENSP00000514791.1:p.Ala487=
ENST00000700093.1:c.1457C= (MASP2)	ENSP00000514792.1:p.Ala486=
ENST00000700094.1:c.1489C= (MASP2)	ENSP00000514793.1:n.1489C=
ENST00000700095.1:c.1298-617C= (MASP2)	ENSP00000514794.1:n.1298-617C=
ENST00000700096.1:c.1101-617C= (MASP2)	ENSP00000514795.1:n.1101-617C=
ENST00000700097.1:c.1509C= (MASP2)	ENSP00000514796.1:n.1509C=
ENST00000400897.8:c.1481C= (MASP2) MANE Select	ENSP00000383690.3:p.Ala494=
ENST00000400897.7:c.1481C= (MASP2)	ENSP00000383690.3:p.Ala494=
ENST00000611136.4:c.448+2257G=
ENST00000612542.1:c.206+2257G=
ENST00000614757.4:c.*452+2257G=	ENSP00000481867.1:n.*452+2257G=
ENST00000620028.1:n.416+2257G=
ENST00000622108.1:c.232-2222G=	ENSP00000480398.1:n.232-2222G=
NM_006610.3:c.1481C= (MASP2)	NP_006601.2:p.Ala494=
XM_017000863.2:c.*3011+1800G= (TARDBP)	XP_016856352.1:n.*3011+1800G=
XM_017000864.2:c.*1895+1800G= (TARDBP)	XP_016856353.1:n.*1895+1800G=
XM_017000865.2:c.*1781-2222G= (TARDBP)	XP_016856354.1:n.*1781-2222G=
NM_006610.4:c.1481C= (MASP2) MANE Select	NP_006601.2:p.Ala494=