Canonical Allele Identifier: CA2135804859
Gene: MGAT2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.49622221_49622222delinsAT , CM000676.2:g.49622221_49622222delinsAT GRCh38
NC_000014.8:g.50088939_50088940delinsAT , CM000676.1:g.50088939_50088940delinsAT GRCh37
NC_000014.7:g.49158689_49158690delinsAT NCBI36
NG_008920.1:g.6451_6452delinsAT
NG_033054.1:g.3410_3411delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000305386.4:c.953_954delinsAT MANE Select ENSP00000307423.2:p.Asn318=
ENST00000305386.3:c.953_954delinsAT ENSP00000307423.2:p.Asn318=
NM_002408.3:c.953_954delinsAT NP_002399.1:p.Asn318=
NM_002408.4:c.953_954delinsAT MANE Select NP_002399.1:p.Asn318=
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