Canonical Allele Identifier: CA338364189

Gene: MASP2 TARDBP

Linked Data

• MyVariant Identifiers: chr1:g.11082223A>G (hg19) ; chr1:g.11022166A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11022166A>G , CM000663.2:g.11022166A>G	GRCh38
NC_000001.10:g.11082223A>G , CM000663.1:g.11082223A>G	GRCh37
NC_000001.9:g.11004810A>G	NCBI36
NG_008734.1:g.14545A>G , LRG_659:g.14545A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700088.1:c.1424T>C (MASP2)	ENSP00000514787.1:n.1424T>C
ENST00000240185.8:c.757A>G (TARDBP) MANE Select	ENSP00000240185.4:p.Ile253Val
ENST00000639083.1:c.757A>G (TARDBP)	ENSP00000491203.1:p.Ile253Val
ENST00000639599.1:c.757A>G (TARDBP)	ENSP00000492196.1:p.Ile253Val
ENST00000649624.1:c.757A>G (TARDBP)	ENSP00000497327.1:p.Ile253Val
ENST00000240185.7:c.757A>G (TARDBP)	ENSP00000240185.3:p.Ile253Val
ENST00000315091.7:c.757A>G (TARDBP)	ENSP00000313129.3:p.Ile253Val
ENST00000439080.6:c.*338A>G (TARDBP)	ENSP00000404666.3:n.*338A>G
ENST00000472476.5:c.*646A>G (TARDBP)	ENSP00000465080.1:n.*646A>G
ENST00000473869.5:c.757A>G (TARDBP)	ENSP00000432132.1:p.Ile253Val
ENST00000477447.6:c.56A>G (TARDBP)
ENST00000610369.4:c.235A>G (TARDBP)	ENSP00000482559.1:p.Ile79Val
ENST00000611136.4:c.137A>G
ENST00000611963.4:c.397A>G (TARDBP)	ENSP00000481330.1:p.Ile133Val
ENST00000612542.1:c.23A>G
ENST00000614494.1:c.210A>G (TARDBP)
ENST00000614757.4:c.757A>G	ENSP00000481867.1:p.Ile253Val
ENST00000616545.4:c.757A>G (TARDBP)	ENSP00000484722.1:p.Ile253Val
ENST00000617172.4:c.498A>G (TARDBP)
ENST00000619555.4:c.308A>G (TARDBP)
ENST00000620632.4:c.308A>G (TARDBP)
ENST00000621715.4:c.586A>G (TARDBP)	ENSP00000480690.1:p.Ile196Val
ENST00000621790.4:c.757A>G (TARDBP)	ENSP00000482191.1:p.Ile253Val
ENST00000622057.4:c.504A>G (TARDBP)
ENST00000629725.2:c.757A>G (TARDBP)	ENSP00000486989.1:p.Ile253Val
NM_007375.3:c.757A>G , LRG_659t1:c.757A>G (TARDBP)	NP_031401.1:p.Ile253Val
XR_946596.1:n.879A>G (TARDBP)
XR_946597.1:n.879A>G (TARDBP)
XM_017000863.2:c.757A>G (TARDBP)	XP_016856352.1:p.Ile253Val
XM_017000864.2:c.757A>G (TARDBP)	XP_016856353.1:p.Ile253Val
XM_017000865.2:c.757A>G (TARDBP)	XP_016856354.1:p.Ile253Val
XM_017000866.2:c.757A>G (TARDBP)	XP_016856355.1:p.Ile253Val
XM_017000867.2:c.757A>G (TARDBP)	XP_016856356.1:p.Ile253Val
XM_017000868.2:c.757A>G (TARDBP)	XP_016856357.1:p.Ile253Val
NM_007375.4:c.757A>G (TARDBP) MANE Select	NP_031401.1:p.Ile253Val