Canonical Allele Identifier: CA2134798335
Gene: MDGA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.47571079_47571080delinsTC , CM000676.2:g.47571079_47571080delinsTC GRCh38
NC_000014.8:g.48040282_48040283delinsTC , CM000676.1:g.48040282_48040283delinsTC GRCh37
NC_000014.7:g.47110032_47110033delinsTC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000399232.8:c.280+103437_280+103438delinsGA MANE Select ENSP00000382178.4:n.280+103437_280+103438delinsGA
ENST00000399232.6:c.73+103437_73+103438delinsGA ENSP00000382178.3:n.73+103437_73+103438delinsGA
ENST00000557238.5:c.-615+55259_-615+55260delinsGA ENSP00000452593.1:n.-615+55259_-615+55260delinsGA
NM_001113498.2:c.73+103437_73+103438delinsGA NP_001106970.3:n.73+103437_73+103438delinsGA
XM_011536520.1:c.280+103437_280+103438delinsGA XP_011534822.1:n.280+103437_280+103438delinsGA
XM_011536521.1:c.280+103437_280+103438delinsGA XP_011534823.1:n.280+103437_280+103438delinsGA
XM_011536522.1:c.280+103437_280+103438delinsGA XP_011534824.1:n.280+103437_280+103438delinsGA
XM_011536523.1:c.280+103437_280+103438delinsGA XP_011534825.1:n.280+103437_280+103438delinsGA
XM_011536522.3:c.280+103437_280+103438delinsGA XP_011534824.1:n.280+103437_280+103438delinsGA
XM_017021061.2:c.280+103437_280+103438delinsGA XP_016876550.1:n.280+103437_280+103438delinsGA
XR_001750175.2:n.800+103437_800+103438delinsGA
NM_001113498.3:c.280+103437_280+103438delinsGA MANE Select NP_001106970.4:n.280+103437_280+103438delinsGA