Canonical Allele Identifier: CA2135804403
Gene: MGAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.49621608_49621609delinsGC , CM000676.2:g.49621608_49621609delinsGC GRCh38
NC_000014.8:g.50088326_50088327delinsGC , CM000676.1:g.50088326_50088327delinsGC GRCh37
NC_000014.7:g.49158076_49158077delinsGC NCBI36
NG_008920.1:g.5838_5839delinsGC
NG_033054.1:g.4023_4024delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000305386.4:c.340_341delinsGC MANE Select ENSP00000307423.2:p.Ala114=
ENST00000305386.3:c.340_341delinsGC ENSP00000307423.2:p.Ala114=
NM_002408.3:c.340_341delinsGC NP_002399.1:p.Ala114=
NM_002408.4:c.340_341delinsGC MANE Select NP_002399.1:p.Ala114=