Canonical Allele Identifier: CA2135804519
Gene: MGAT2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.49621692_49621693delinsCA , CM000676.2:g.49621692_49621693delinsCA GRCh38
NC_000014.8:g.50088410_50088411delinsCA , CM000676.1:g.50088410_50088411delinsCA GRCh37
NC_000014.7:g.49158160_49158161delinsCA NCBI36
NG_008920.1:g.5922_5923delinsCA
NG_033054.1:g.3939_3940delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000305386.4:c.424_425delinsCA MANE Select ENSP00000307423.2:p.Gln142=
ENST00000305386.3:c.424_425delinsCA ENSP00000307423.2:p.Gln142=
NM_002408.3:c.424_425delinsCA NP_002399.1:p.Gln142=
NM_002408.4:c.424_425delinsCA MANE Select NP_002399.1:p.Gln142=
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