Canonical Allele Identifier: CA1153469060

Gene: MASP2 TARDBP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11027480T= , CM000663.2:g.11027480T=	GRCh38
NC_000001.10:g.11087537T= , CM000663.1:g.11087537T=	GRCh37
NC_000001.9:g.11010124T=	NCBI36
NG_007289.1:g.24749A=
NG_008734.1:g.19859T= , LRG_659:g.19859T=
NG_007289.2:g.24749A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699927.1:n.405A= (MASP2)
ENST00000699958.1:c.1361A= (MASP2)	ENSP00000514717.1:p.Lys454=
ENST00000700088.1:c.1298-632A= (MASP2)	ENSP00000514787.1:n.1298-632A=
ENST00000700089.1:c.1463A= (MASP2)	ENSP00000514788.1:n.1463A=
ENST00000700090.1:c.1345A= (MASP2)	ENSP00000514789.1:n.1345A=
ENST00000700091.1:c.1268A= (MASP2)	ENSP00000514790.1:p.Lys423=
ENST00000700092.1:c.1445A= (MASP2)	ENSP00000514791.1:p.Lys482=
ENST00000700093.1:c.1442A= (MASP2)	ENSP00000514792.1:p.Lys481=
ENST00000700094.1:c.1474A= (MASP2)	ENSP00000514793.1:n.1474A=
ENST00000700095.1:c.1298-632A= (MASP2)	ENSP00000514794.1:n.1298-632A=
ENST00000700096.1:c.1101-632A= (MASP2)	ENSP00000514795.1:n.1101-632A=
ENST00000700097.1:c.1494A= (MASP2)	ENSP00000514796.1:n.1494A=
ENST00000400897.8:c.1466A= (MASP2) MANE Select	ENSP00000383690.3:p.Lys489=
ENST00000400897.7:c.1466A= (MASP2)	ENSP00000383690.3:p.Lys489=
ENST00000611136.4:c.448+2272T=
ENST00000612542.1:c.206+2272T=
ENST00000614757.4:c.*452+2272T=	ENSP00000481867.1:n.*452+2272T=
ENST00000620028.1:n.416+2272T=
ENST00000622108.1:c.232-2207T=	ENSP00000480398.1:n.232-2207T=
NM_006610.3:c.1466A= (MASP2)	NP_006601.2:p.Lys489=
XM_017000863.2:c.*3011+1815T= (TARDBP)	XP_016856352.1:n.*3011+1815T=
XM_017000864.2:c.*1895+1815T= (TARDBP)	XP_016856353.1:n.*1895+1815T=
XM_017000865.2:c.*1781-2207T= (TARDBP)	XP_016856354.1:n.*1781-2207T=
NM_006610.4:c.1466A= (MASP2) MANE Select	NP_006601.2:p.Lys489=