Canonical Allele Identifier: CA338374418

Gene: MASP2 TARDBP

Linked Data

• MyVariant Identifiers: chr1:g.11087462G>T (hg19) ; chr1:g.11027405G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11027405G>T , CM000663.2:g.11027405G>T	GRCh38
NC_000001.10:g.11087462G>T , CM000663.1:g.11087462G>T	GRCh37
NC_000001.9:g.11010049G>T	NCBI36
NG_007289.1:g.24824C>A
NG_008734.1:g.19784G>T , LRG_659:g.19784G>T
NG_007289.2:g.24824C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699927.1:n.480C>A (MASP2)
ENST00000699958.1:c.1436C>A (MASP2)	ENSP00000514717.1:p.Ser479Tyr
ENST00000700088.1:c.1298-557C>A (MASP2)	ENSP00000514787.1:n.1298-557C>A
ENST00000700089.1:c.1538C>A (MASP2)	ENSP00000514788.1:n.1538C>A
ENST00000700090.1:c.1420C>A (MASP2)	ENSP00000514789.1:n.1420C>A
ENST00000700091.1:c.1343C>A (MASP2)	ENSP00000514790.1:p.Ser448Tyr
ENST00000700092.1:c.1520C>A (MASP2)	ENSP00000514791.1:p.Ser507Tyr
ENST00000700093.1:c.1517C>A (MASP2)	ENSP00000514792.1:p.Ser506Tyr
ENST00000700094.1:c.1549C>A (MASP2)	ENSP00000514793.1:n.1549C>A
ENST00000700095.1:c.1298-557C>A (MASP2)	ENSP00000514794.1:n.1298-557C>A
ENST00000700096.1:c.1101-557C>A (MASP2)	ENSP00000514795.1:n.1101-557C>A
ENST00000700097.1:c.1569C>A (MASP2)	ENSP00000514796.1:n.1569C>A
ENST00000400897.8:c.1541C>A (MASP2) MANE Select	ENSP00000383690.3:p.Ser514Tyr
ENST00000400897.7:c.1541C>A (MASP2)	ENSP00000383690.3:p.Ser514Tyr
ENST00000611136.4:c.448+2197G>T
ENST00000612542.1:c.206+2197G>T
ENST00000614757.4:c.*452+2197G>T	ENSP00000481867.1:n.*452+2197G>T
ENST00000620028.1:n.416+2197G>T
ENST00000622108.1:c.231+2197G>T	ENSP00000480398.1:n.231+2197G>T
NM_006610.3:c.1541C>A (MASP2)	NP_006601.2:p.Ser514Tyr
XM_017000863.2:c.*3011+1740G>T (TARDBP)	XP_016856352.1:n.*3011+1740G>T
XM_017000864.2:c.*1895+1740G>T (TARDBP)	XP_016856353.1:n.*1895+1740G>T
XM_017000865.2:c.*1780+2197G>T (TARDBP)	XP_016856354.1:n.*1780+2197G>T
NM_006610.4:c.1541C>A (MASP2) MANE Select	NP_006601.2:p.Ser514Tyr