Canonical Allele Identifier: CA338364261
Gene: MASP2 HGNC NCBI
TARDBP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11022198G>C , CM000663.2:g.11022198G>C GRCh38
NC_000001.10:g.11082255G>C , CM000663.1:g.11082255G>C GRCh37
NC_000001.9:g.11004842G>C NCBI36
NG_008734.1:g.14577G>C , LRG_659:g.14577G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000700088.1:c.1397-5C>G (MASP2) ENSP00000514787.1:n.1397-5C>G
ENST00000240185.8:c.789G>C (TARDBP) MANE Select ENSP00000240185.4:p.Lys263Asn
ENST00000639083.1:c.789G>C (TARDBP) ENSP00000491203.1:p.Lys263Asn
ENST00000639599.1:c.789G>C (TARDBP) ENSP00000492196.1:p.Lys263Asn
ENST00000649624.1:c.768+21G>C (TARDBP) ENSP00000497327.1:n.768+21G>C
ENST00000240185.7:c.789G>C (TARDBP) ENSP00000240185.3:p.Lys263Asn
ENST00000315091.7:c.789G>C (TARDBP) ENSP00000313129.3:p.Lys263Asn
ENST00000439080.6:c.*370G>C (TARDBP) ENSP00000404666.3:n.*370G>C
ENST00000473869.5:c.789G>C (TARDBP) ENSP00000432132.1:p.Lys263Asn
ENST00000477447.6:c.88G>C (TARDBP)
ENST00000610369.4:c.267G>C (TARDBP) ENSP00000482559.1:p.Lys89Asn
ENST00000611136.4:c.169G>C
ENST00000611963.4:c.429G>C (TARDBP) ENSP00000481330.1:p.Lys143Asn
ENST00000612542.1:c.55G>C
ENST00000614494.1:c.221+21G>C (TARDBP)
ENST00000614757.4:c.789G>C ENSP00000481867.1:p.Lys263Asn
ENST00000616545.4:c.789G>C (TARDBP) ENSP00000484722.1:p.Lys263Asn
ENST00000617172.4:c.530G>C (TARDBP)
ENST00000619555.4:c.340G>C (TARDBP)
ENST00000620632.4:c.340G>C (TARDBP)
ENST00000621715.4:c.618G>C (TARDBP) ENSP00000480690.1:p.Lys206Asn
ENST00000621790.4:c.789G>C (TARDBP) ENSP00000482191.1:p.Lys263Asn
ENST00000622057.4:c.536G>C (TARDBP)
ENST00000629725.2:c.789G>C (TARDBP) ENSP00000486989.1:p.Lys263Asn
NM_007375.3:c.789G>C , LRG_659t1:c.789G>C (TARDBP) NP_031401.1:p.Lys263Asn
XR_946596.1:n.911G>C (TARDBP)
XR_946597.1:n.911G>C (TARDBP)
XM_017000863.2:c.789G>C (TARDBP) XP_016856352.1:p.Lys263Asn
XM_017000864.2:c.789G>C (TARDBP) XP_016856353.1:p.Lys263Asn
XM_017000865.2:c.789G>C (TARDBP) XP_016856354.1:p.Lys263Asn
XM_017000866.2:c.789G>C (TARDBP) XP_016856355.1:p.Lys263Asn
XM_017000867.2:c.789G>C (TARDBP) XP_016856356.1:p.Lys263Asn
XM_017000868.2:c.789G>C (TARDBP) XP_016856357.1:p.Lys263Asn
NM_007375.4:c.789G>C (TARDBP) MANE Select NP_031401.1:p.Lys263Asn