Canonical Allele Identifier: CA1149041615
Gene: MASP2 HGNC NCBI
TARDBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11022267G= , CM000663.2:g.11022267G= GRCh38
NC_000001.10:g.11082324G= , CM000663.1:g.11082324G= GRCh37
NC_000001.9:g.11004911G= NCBI36
NG_008734.1:g.14646G= , LRG_659:g.14646G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700088.1:c.1397-74C= (MASP2) ENSP00000514787.1:n.1397-74C=
ENST00000240185.8:c.858G= (TARDBP) MANE Select ENSP00000240185.4:p.Gln286=
ENST00000639083.1:c.858G= (TARDBP) ENSP00000491203.1:p.Gln286=
ENST00000639599.1:c.832+26G= (TARDBP) ENSP00000492196.1:n.832+26G=
ENST00000649624.1:c.768+90G= (TARDBP) ENSP00000497327.1:n.768+90G=
ENST00000240185.7:c.858G= (TARDBP) ENSP00000240185.3:p.Gln286=
ENST00000315091.7:c.832+26G= (TARDBP) ENSP00000313129.3:n.832+26G=
ENST00000439080.6:c.*439G= (TARDBP) ENSP00000404666.3:n.*439G=
ENST00000473869.5:c.841+17G= (TARDBP) ENSP00000432132.1:n.841+17G=
ENST00000477447.6:c.140+17G= (TARDBP)
ENST00000610369.4:c.319+17G= (TARDBP) ENSP00000482559.1:n.319+17G=
ENST00000611136.4:c.212+26G=
ENST00000611963.4:c.472+26G= (TARDBP) ENSP00000481330.1:n.472+26G=
ENST00000612542.1:c.107+17G=
ENST00000614494.1:c.221+90G= (TARDBP)
ENST00000614757.4:c.841+17G= ENSP00000481867.1:n.841+17G=
ENST00000616545.4:c.841+17G= (TARDBP) ENSP00000484722.1:n.841+17G=
ENST00000617172.4:c.582+17G= (TARDBP)
ENST00000619555.4:c.392+17G= (TARDBP)
ENST00000620632.4:c.392+17G= (TARDBP)
ENST00000621715.4:c.687G= (TARDBP) ENSP00000480690.1:p.Gln229=
ENST00000621790.4:c.858G= (TARDBP) ENSP00000482191.1:p.Gln286=
ENST00000622057.4:c.579+26G= (TARDBP)
ENST00000629725.2:c.841+17G= (TARDBP) ENSP00000486989.1:n.841+17G=
NM_007375.3:c.858G= , LRG_659t1:c.858G= (TARDBP) NP_031401.1:p.Gln286=
XR_946596.1:n.980G= (TARDBP)
XR_946597.1:n.980G= (TARDBP)
XM_017000863.2:c.858G= (TARDBP) XP_016856352.1:p.Gln286=
XM_017000864.2:c.858G= (TARDBP) XP_016856353.1:p.Gln286=
XM_017000865.2:c.858G= (TARDBP) XP_016856354.1:p.Gln286=
XM_017000866.2:c.858G= (TARDBP) XP_016856355.1:p.Gln286=
XM_017000867.2:c.858G= (TARDBP) XP_016856356.1:p.Gln286=
XM_017000868.2:c.858G= (TARDBP) XP_016856357.1:p.Gln286=
NM_007375.4:c.858G= (TARDBP) MANE Select NP_031401.1:p.Gln286=