Canonical Allele Identifier: CA2134629904
Gene: MDGA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.47216712A= , CM000676.2:g.47216712A= GRCh38
NC_000014.8:g.47685915A= , CM000676.1:g.47685915A= GRCh37
NC_000014.7:g.46755665A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000399232.8:c.595+1309T= MANE Select ENSP00000382178.4:n.595+1309T=
ENST00000426342.7:c.-3+1309T= ENSP00000405456.4:n.-3+1309T=
ENST00000357362.7:c.-300+1309T= ENSP00000349925.3:n.-300+1309T=
ENST00000399232.6:c.388+1309T= ENSP00000382178.3:n.388+1309T=
ENST00000426342.5:c.-3+1309T= ENSP00000405456.2:n.-3+1309T=
ENST00000482848.7:c.-300+1309T= ENSP00000434991.2:n.-300+1309T=
ENST00000557238.5:c.-300+1309T= ENSP00000452593.1:n.-300+1309T=
NM_001113498.2:c.388+1309T= NP_001106970.3:n.388+1309T=
NM_182830.4:c.-300+1309T= NP_878250.2:n.-300+1309T=
NR_103766.1:n.459+1309T=
XM_011536519.1:c.460+1309T= XP_011534821.1:n.460+1309T=
XM_011536520.1:c.595+1309T= XP_011534822.1:n.595+1309T=
XM_011536521.1:c.595+1309T= XP_011534823.1:n.595+1309T=
XM_011536522.1:c.595+1309T= XP_011534824.1:n.595+1309T=
XM_011536523.1:c.595+1309T= XP_011534825.1:n.595+1309T=
XM_011536519.2:c.460+1309T= XP_011534821.1:n.460+1309T=
XM_011536522.3:c.595+1309T= XP_011534824.1:n.595+1309T=
XM_017021061.2:c.595+1309T= XP_016876550.1:n.595+1309T=
XR_001750175.2:n.1115+1309T=
NM_001113498.3:c.595+1309T= MANE Select NP_001106970.4:n.595+1309T=
NR_103766.2:n.459+1309T=