Canonical Allele Identifier: CA1142369833

Gene: MASP2 TARDBP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11027555C= , CM000663.2:g.11027555C=	GRCh38
NC_000001.10:g.11087612C= , CM000663.1:g.11087612C=	GRCh37
NC_000001.9:g.11010199C=	NCBI36
NG_007289.1:g.24674G=
NG_007289.2:g.24674G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699927.1:n.330G= (MASP2)
ENST00000699958.1:c.1286G= (MASP2)	ENSP00000514717.1:p.Gly429=
ENST00000700088.1:c.1298-707G= (MASP2)	ENSP00000514787.1:n.1298-707G=
ENST00000700089.1:c.1388G= (MASP2)	ENSP00000514788.1:n.1388G=
ENST00000700090.1:c.1270G= (MASP2)	ENSP00000514789.1:n.1270G=
ENST00000700091.1:c.1193G= (MASP2)	ENSP00000514790.1:p.Gly398=
ENST00000700092.1:c.1370G= (MASP2)	ENSP00000514791.1:p.Gly457=
ENST00000700093.1:c.1367G= (MASP2)	ENSP00000514792.1:p.Gly456=
ENST00000700094.1:c.1399G= (MASP2)	ENSP00000514793.1:n.1399G=
ENST00000700095.1:c.1298-707G= (MASP2)	ENSP00000514794.1:n.1298-707G=
ENST00000700096.1:c.1101-707G= (MASP2)	ENSP00000514795.1:n.1101-707G=
ENST00000700097.1:c.1419G= (MASP2)	ENSP00000514796.1:n.1419G=
ENST00000400897.8:c.1391G= (MASP2) MANE Select	ENSP00000383690.3:p.Gly464=
ENST00000400897.7:c.1391G= (MASP2)	ENSP00000383690.3:p.Gly464=
ENST00000611136.4:c.448+2347C=
ENST00000612542.1:c.206+2347C=
ENST00000614757.4:c.*452+2347C=	ENSP00000481867.1:n.*452+2347C=
ENST00000620028.1:n.416+2347C=
ENST00000622108.1:c.232-2132C=	ENSP00000480398.1:n.232-2132C=
NM_006610.3:c.1391G= (MASP2)	NP_006601.2:p.Gly464=
XM_017000863.2:c.*3011+1890C= (TARDBP)	XP_016856352.1:n.*3011+1890C=
XM_017000864.2:c.*1895+1890C= (TARDBP)	XP_016856353.1:n.*1895+1890C=
XM_017000865.2:c.*1781-2132C= (TARDBP)	XP_016856354.1:n.*1781-2132C=
NM_006610.4:c.1391G= (MASP2) MANE Select	NP_006601.2:p.Gly464=