Canonical Allele Identifier: CA338364097
Gene: MASP2 HGNC NCBI
TARDBP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11022127G>A , CM000663.2:g.11022127G>A GRCh38
NC_000001.10:g.11082184G>A , CM000663.1:g.11082184G>A GRCh37
NC_000001.9:g.11004771G>A NCBI36
NG_008734.1:g.14506G>A , LRG_659:g.14506G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000700088.1:c.1463C>T (MASP2) ENSP00000514787.1:n.1463C>T
ENST00000240185.8:c.718G>A (TARDBP) MANE Select ENSP00000240185.4:p.Ala240Thr
ENST00000639083.1:c.718G>A (TARDBP) ENSP00000491203.1:p.Ala240Thr
ENST00000639599.1:c.718G>A (TARDBP) ENSP00000492196.1:p.Ala240Thr
ENST00000649624.1:c.718G>A (TARDBP) ENSP00000497327.1:p.Ala240Thr
ENST00000240185.7:c.718G>A (TARDBP) ENSP00000240185.3:p.Ala240Thr
ENST00000315091.7:c.718G>A (TARDBP) ENSP00000313129.3:p.Ala240Thr
ENST00000439080.6:c.*299G>A (TARDBP) ENSP00000404666.3:n.*299G>A
ENST00000472476.5:c.*607G>A (TARDBP) ENSP00000465080.1:n.*607G>A
ENST00000473869.5:c.718G>A (TARDBP) ENSP00000432132.1:p.Ala240Thr
ENST00000477447.6:c.17G>A (TARDBP)
ENST00000610369.4:c.196G>A (TARDBP) ENSP00000482559.1:p.Ala66Thr
ENST00000611136.4:c.98G>A
ENST00000611963.4:c.358G>A (TARDBP) ENSP00000481330.1:p.Ala120Thr
ENST00000614494.1:c.171G>A (TARDBP)
ENST00000614757.4:c.718G>A ENSP00000481867.1:p.Ala240Thr
ENST00000616545.4:c.718G>A (TARDBP) ENSP00000484722.1:p.Ala240Thr
ENST00000617172.4:c.459G>A (TARDBP)
ENST00000619555.4:c.269G>A (TARDBP)
ENST00000620632.4:c.269G>A (TARDBP)
ENST00000621715.4:c.547G>A (TARDBP) ENSP00000480690.1:p.Ala183Thr
ENST00000621790.4:c.718G>A (TARDBP) ENSP00000482191.1:p.Ala240Thr
ENST00000622057.4:c.465G>A (TARDBP)
ENST00000629725.2:c.718G>A (TARDBP) ENSP00000486989.1:p.Ala240Thr
NM_007375.3:c.718G>A , LRG_659t1:c.718G>A (TARDBP) NP_031401.1:p.Ala240Thr
XR_946596.1:n.840G>A (TARDBP)
XR_946597.1:n.840G>A (TARDBP)
XM_017000863.2:c.718G>A (TARDBP) XP_016856352.1:p.Ala240Thr
XM_017000864.2:c.718G>A (TARDBP) XP_016856353.1:p.Ala240Thr
XM_017000865.2:c.718G>A (TARDBP) XP_016856354.1:p.Ala240Thr
XM_017000866.2:c.718G>A (TARDBP) XP_016856355.1:p.Ala240Thr
XM_017000867.2:c.718G>A (TARDBP) XP_016856356.1:p.Ala240Thr
XM_017000868.2:c.718G>A (TARDBP) XP_016856357.1:p.Ala240Thr
NM_007375.4:c.718G>A (TARDBP) MANE Select NP_031401.1:p.Ala240Thr