Canonical Allele Identifier: CA2573130260

Gene: MASP2 TARDBP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11022542_11022556del , CM000663.2:g.11022542_11022556del	GRCh38
NC_000001.10:g.11082599_11082613del , CM000663.1:g.11082599_11082613del	GRCh37
NC_000001.9:g.11005186_11005200del	NCBI36
NG_008734.1:g.14921_14935del , LRG_659:g.14921_14935del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700088.1:c.1397-362_1397-348del (MASP2)	ENSP00000514787.1:n.1397-362_1397-348del
ENST00000240185.8:c.1133_1147del (TARDBP) MANE Select	ENSP00000240185.4:p.Asn378_Ala382del
ENST00000639083.1:c.1133_1147del (TARDBP)	ENSP00000491203.1:p.Asn378_Ala382del
ENST00000639599.1:c.832+301_832+315del (TARDBP)	ENSP00000492196.1:n.832+301_832+315del
ENST00000649624.1:c.768+365_768+379del (TARDBP)	ENSP00000497327.1:n.768+365_768+379del
ENST00000240185.7:c.1133_1147del (TARDBP)	ENSP00000240185.3:p.Asn378_Ala382del
ENST00000315091.7:c.832+301_832+315del (TARDBP)	ENSP00000313129.3:n.832+301_832+315del
ENST00000439080.6:c.*714_*728del (TARDBP)	ENSP00000404666.3:n.*714_*728del
ENST00000473869.5:c.841+292_841+306del (TARDBP)	ENSP00000432132.1:n.841+292_841+306del
ENST00000477447.6:c.140+292_140+306del (TARDBP)
ENST00000610369.4:c.319+292_319+306del (TARDBP)	ENSP00000482559.1:n.319+292_319+306del
ENST00000611136.4:c.212+301_212+315del
ENST00000611963.4:c.472+301_472+315del (TARDBP)	ENSP00000481330.1:n.472+301_472+315del
ENST00000612542.1:c.107+292_107+306del
ENST00000614494.1:c.221+365_221+379del (TARDBP)
ENST00000614757.4:c.841+292_841+306del	ENSP00000481867.1:n.841+292_841+306del
ENST00000616545.4:c.841+292_841+306del (TARDBP)	ENSP00000484722.1:n.841+292_841+306del
ENST00000617172.4:c.582+292_582+306del (TARDBP)
ENST00000619555.4:c.392+292_392+306del (TARDBP)
ENST00000620505.1:c.235_249del (TARDBP)
ENST00000620632.4:c.392+292_392+306del (TARDBP)
ENST00000621790.4:c.859+274_859+288del (TARDBP)	ENSP00000482191.1:n.859+274_859+288del
ENST00000622057.4:c.579+301_579+315del (TARDBP)
ENST00000629725.2:c.841+292_841+306del (TARDBP)	ENSP00000486989.1:n.841+292_841+306del
NM_007375.3:c.1133_1147del , LRG_659t1:c.1133_1147del (TARDBP)	NP_031401.1:p.Asn378_Ala382del
XR_946596.1:n.1255_1269del (TARDBP)
XR_946597.1:n.1255_1269del (TARDBP)
XM_017000863.2:c.1133_1147del (TARDBP)	XP_016856352.1:p.Asn378_Ala382del
XM_017000864.2:c.1133_1147del (TARDBP)	XP_016856353.1:p.Asn378_Ala382del
XM_017000865.2:c.1133_1147del (TARDBP)	XP_016856354.1:p.Asn378_Ala382del
XM_017000866.2:c.1133_1147del (TARDBP)	XP_016856355.1:p.Asn378_Ala382del
XM_017000867.2:c.1133_1147del (TARDBP)	XP_016856356.1:p.Asn378_Ala382del
XM_017000868.2:c.1133_1147del (TARDBP)	XP_016856357.1:p.Asn378_Ala382del
NM_007375.4:c.1133_1147del (TARDBP) MANE Select	NP_031401.1:p.Asn378_Ala382del