Canonical Allele Identifier: CA706298316
Gene: MDGA2 HGNC NCBI

Linked Data

dbSNP Id: rs1276448425

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.47216618_47216619del , CM000676.2:g.47216618_47216619del GRCh38
NC_000014.8:g.47685821_47685822del , CM000676.1:g.47685821_47685822del GRCh37
NC_000014.7:g.46755571_46755572del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000399232.8:c.595+1405_595+1406del MANE Select ENSP00000382178.4:n.595+1405_595+1406del
ENST00000426342.7:c.-3+1405_-3+1406del ENSP00000405456.4:n.-3+1405_-3+1406del
ENST00000357362.7:c.-300+1405_-300+1406del ENSP00000349925.3:n.-300+1405_-300+1406del
ENST00000399232.6:c.388+1405_388+1406del ENSP00000382178.3:n.388+1405_388+1406del
ENST00000426342.5:c.-3+1405_-3+1406del ENSP00000405456.2:n.-3+1405_-3+1406del
ENST00000482848.7:c.-300+1405_-300+1406del ENSP00000434991.2:n.-300+1405_-300+1406del
ENST00000557238.5:c.-300+1405_-300+1406del ENSP00000452593.1:n.-300+1405_-300+1406del
NM_001113498.2:c.388+1405_388+1406del NP_001106970.3:n.388+1405_388+1406del
NM_182830.4:c.-300+1405_-300+1406del NP_878250.2:n.-300+1405_-300+1406del
NR_103766.1:n.459+1405_459+1406del
XM_011536519.1:c.460+1405_460+1406del XP_011534821.1:n.460+1405_460+1406del
XM_011536520.1:c.595+1405_595+1406del XP_011534822.1:n.595+1405_595+1406del
XM_011536521.1:c.595+1405_595+1406del XP_011534823.1:n.595+1405_595+1406del
XM_011536522.1:c.595+1405_595+1406del XP_011534824.1:n.595+1405_595+1406del
XM_011536523.1:c.595+1405_595+1406del XP_011534825.1:n.595+1405_595+1406del
XM_011536519.2:c.460+1405_460+1406del XP_011534821.1:n.460+1405_460+1406del
XM_011536522.3:c.595+1405_595+1406del XP_011534824.1:n.595+1405_595+1406del
XM_017021061.2:c.595+1405_595+1406del XP_016876550.1:n.595+1405_595+1406del
XR_001750175.2:n.1115+1405_1115+1406del
NM_001113498.3:c.595+1405_595+1406del MANE Select NP_001106970.4:n.595+1405_595+1406del
NR_103766.2:n.459+1405_459+1406del