Canonical Allele Identifier: CA2134695545
Gene: MDGA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.47355251_47355252delinsTG , CM000676.2:g.47355251_47355252delinsTG GRCh38
NC_000014.8:g.47824454_47824455delinsTG , CM000676.1:g.47824454_47824455delinsTG GRCh37
NC_000014.7:g.46894204_46894205delinsTG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000399232.8:c.281-53702_281-53701delinsCA MANE Select ENSP00000382178.4:n.281-53702_281-53701delinsCA
ENST00000399232.6:c.74-53702_74-53701delinsCA ENSP00000382178.3:n.74-53702_74-53701delinsCA
ENST00000557238.5:c.-614-53702_-614-53701delinsCA ENSP00000452593.1:n.-614-53702_-614-53701delinsCA
NM_001113498.2:c.74-53702_74-53701delinsCA NP_001106970.3:n.74-53702_74-53701delinsCA
XM_011536520.1:c.281-53702_281-53701delinsCA XP_011534822.1:n.281-53702_281-53701delinsCA
XM_011536521.1:c.281-53702_281-53701delinsCA XP_011534823.1:n.281-53702_281-53701delinsCA
XM_011536522.1:c.281-53702_281-53701delinsCA XP_011534824.1:n.281-53702_281-53701delinsCA
XM_011536523.1:c.281-53702_281-53701delinsCA XP_011534825.1:n.281-53702_281-53701delinsCA
XM_011536522.3:c.281-53702_281-53701delinsCA XP_011534824.1:n.281-53702_281-53701delinsCA
XM_017021061.2:c.281-53702_281-53701delinsCA XP_016876550.1:n.281-53702_281-53701delinsCA
XR_001750175.2:n.801-53702_801-53701delinsCA
NM_001113498.3:c.281-53702_281-53701delinsCA MANE Select NP_001106970.4:n.281-53702_281-53701delinsCA