Canonical Allele Identifier: CA1153469142

Gene: MASP2 TARDBP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11027535C= , CM000663.2:g.11027535C=	GRCh38
NC_000001.10:g.11087592C= , CM000663.1:g.11087592C=	GRCh37
NC_000001.9:g.11010179C=	NCBI36
NG_007289.1:g.24694G=
NG_007289.2:g.24694G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699927.1:n.350G= (MASP2)
ENST00000699958.1:c.1306G= (MASP2)	ENSP00000514717.1:p.Ala436=
ENST00000700088.1:c.1298-687G= (MASP2)	ENSP00000514787.1:n.1298-687G=
ENST00000700089.1:c.1408G= (MASP2)	ENSP00000514788.1:n.1408G=
ENST00000700090.1:c.1290G= (MASP2)	ENSP00000514789.1:n.1290G=
ENST00000700091.1:c.1213G= (MASP2)	ENSP00000514790.1:p.Ala405=
ENST00000700092.1:c.1390G= (MASP2)	ENSP00000514791.1:p.Ala464=
ENST00000700093.1:c.1387G= (MASP2)	ENSP00000514792.1:p.Ala463=
ENST00000700094.1:c.1419G= (MASP2)	ENSP00000514793.1:n.1419G=
ENST00000700095.1:c.1298-687G= (MASP2)	ENSP00000514794.1:n.1298-687G=
ENST00000700096.1:c.1101-687G= (MASP2)	ENSP00000514795.1:n.1101-687G=
ENST00000700097.1:c.1439G= (MASP2)	ENSP00000514796.1:n.1439G=
ENST00000400897.8:c.1411G= (MASP2) MANE Select	ENSP00000383690.3:p.Ala471=
ENST00000400897.7:c.1411G= (MASP2)	ENSP00000383690.3:p.Ala471=
ENST00000611136.4:c.448+2327C=
ENST00000612542.1:c.206+2327C=
ENST00000614757.4:c.*452+2327C=	ENSP00000481867.1:n.*452+2327C=
ENST00000620028.1:n.416+2327C=
ENST00000622108.1:c.232-2152C=	ENSP00000480398.1:n.232-2152C=
NM_006610.3:c.1411G= (MASP2)	NP_006601.2:p.Ala471=
XM_017000863.2:c.*3011+1870C= (TARDBP)	XP_016856352.1:n.*3011+1870C=
XM_017000864.2:c.*1895+1870C= (TARDBP)	XP_016856353.1:n.*1895+1870C=
XM_017000865.2:c.*1781-2152C= (TARDBP)	XP_016856354.1:n.*1781-2152C=
NM_006610.4:c.1411G= (MASP2) MANE Select	NP_006601.2:p.Ala471=