Canonical Allele Identifier: CA338375398

Gene: MASP2 TARDBP

Linked Data

• dbSNP Id: rs1483758522
• gnomAD v2: 1-11087598-C-G
• MyVariant Identifiers: chr1:g.11087598C>G (hg19) ; chr1:g.11027541C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11027541C>G , CM000663.2:g.11027541C>G	GRCh38
NC_000001.10:g.11087598C>G , CM000663.1:g.11087598C>G	GRCh37
NC_000001.9:g.11010185C>G	NCBI36
NG_007289.1:g.24688G>C
NG_007289.2:g.24688G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699927.1:n.344G>C (MASP2)
ENST00000699958.1:c.1300G>C (MASP2)	ENSP00000514717.1:p.Ala434Pro
ENST00000700088.1:c.1298-693G>C (MASP2)	ENSP00000514787.1:n.1298-693G>C
ENST00000700089.1:c.1402G>C (MASP2)	ENSP00000514788.1:n.1402G>C
ENST00000700090.1:c.1284G>C (MASP2)	ENSP00000514789.1:n.1284G>C
ENST00000700091.1:c.1207G>C (MASP2)	ENSP00000514790.1:p.Ala403Pro
ENST00000700092.1:c.1384G>C (MASP2)	ENSP00000514791.1:p.Ala462Pro
ENST00000700093.1:c.1381G>C (MASP2)	ENSP00000514792.1:p.Ala461Pro
ENST00000700094.1:c.1413G>C (MASP2)	ENSP00000514793.1:n.1413G>C
ENST00000700095.1:c.1298-693G>C (MASP2)	ENSP00000514794.1:n.1298-693G>C
ENST00000700096.1:c.1101-693G>C (MASP2)	ENSP00000514795.1:n.1101-693G>C
ENST00000700097.1:c.1433G>C (MASP2)	ENSP00000514796.1:n.1433G>C
ENST00000400897.8:c.1405G>C (MASP2) MANE Select	ENSP00000383690.3:p.Ala469Pro
ENST00000400897.7:c.1405G>C (MASP2)	ENSP00000383690.3:p.Ala469Pro
ENST00000611136.4:c.448+2333C>G
ENST00000612542.1:c.206+2333C>G
ENST00000614757.4:c.*452+2333C>G	ENSP00000481867.1:n.*452+2333C>G
ENST00000620028.1:n.416+2333C>G
ENST00000622108.1:c.232-2146C>G	ENSP00000480398.1:n.232-2146C>G
NM_006610.3:c.1405G>C (MASP2)	NP_006601.2:p.Ala469Pro
XM_017000863.2:c.*3011+1876C>G (TARDBP)	XP_016856352.1:n.*3011+1876C>G
XM_017000864.2:c.*1895+1876C>G (TARDBP)	XP_016856353.1:n.*1895+1876C>G
XM_017000865.2:c.*1781-2146C>G (TARDBP)	XP_016856354.1:n.*1781-2146C>G
NM_006610.4:c.1405G>C (MASP2) MANE Select	NP_006601.2:p.Ala469Pro