Canonical Allele Identifier: CA338375017

Gene: MASP2 TARDBP

Linked Data

• MyVariant Identifiers: chr1:g.11087562C>A (hg19) ; chr1:g.11027505C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11027505C>A , CM000663.2:g.11027505C>A	GRCh38
NC_000001.10:g.11087562C>A , CM000663.1:g.11087562C>A	GRCh37
NC_000001.9:g.11010149C>A	NCBI36
NG_007289.1:g.24724G>T
NG_007289.2:g.24724G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699927.1:n.380G>T (MASP2)
ENST00000699958.1:c.1336G>T (MASP2)	ENSP00000514717.1:p.Ala446Ser
ENST00000700088.1:c.1298-657G>T (MASP2)	ENSP00000514787.1:n.1298-657G>T
ENST00000700089.1:c.1438G>T (MASP2)	ENSP00000514788.1:n.1438G>T
ENST00000700090.1:c.1320G>T (MASP2)	ENSP00000514789.1:n.1320G>T
ENST00000700091.1:c.1243G>T (MASP2)	ENSP00000514790.1:p.Ala415Ser
ENST00000700092.1:c.1420G>T (MASP2)	ENSP00000514791.1:p.Ala474Ser
ENST00000700093.1:c.1417G>T (MASP2)	ENSP00000514792.1:p.Ala473Ser
ENST00000700094.1:c.1449G>T (MASP2)	ENSP00000514793.1:n.1449G>T
ENST00000700095.1:c.1298-657G>T (MASP2)	ENSP00000514794.1:n.1298-657G>T
ENST00000700096.1:c.1101-657G>T (MASP2)	ENSP00000514795.1:n.1101-657G>T
ENST00000700097.1:c.1469G>T (MASP2)	ENSP00000514796.1:n.1469G>T
ENST00000400897.8:c.1441G>T (MASP2) MANE Select	ENSP00000383690.3:p.Ala481Ser
ENST00000400897.7:c.1441G>T (MASP2)	ENSP00000383690.3:p.Ala481Ser
ENST00000611136.4:c.448+2297C>A
ENST00000612542.1:c.206+2297C>A
ENST00000614757.4:c.*452+2297C>A	ENSP00000481867.1:n.*452+2297C>A
ENST00000620028.1:n.416+2297C>A
ENST00000622108.1:c.232-2182C>A	ENSP00000480398.1:n.232-2182C>A
NM_006610.3:c.1441G>T (MASP2)	NP_006601.2:p.Ala481Ser
XM_017000863.2:c.*3011+1840C>A (TARDBP)	XP_016856352.1:n.*3011+1840C>A
XM_017000864.2:c.*1895+1840C>A (TARDBP)	XP_016856353.1:n.*1895+1840C>A
XM_017000865.2:c.*1781-2182C>A (TARDBP)	XP_016856354.1:n.*1781-2182C>A
NM_006610.4:c.1441G>T (MASP2) MANE Select	NP_006601.2:p.Ala481Ser