Canonical Allele Identifier: CA2135804851

Gene: MGAT2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.49622212_49622214delinsCAG , CM000676.2:g.49622212_49622214delinsCAG	GRCh38
NC_000014.8:g.50088930_50088932delinsCAG , CM000676.1:g.50088930_50088932delinsCAG	GRCh37
NC_000014.7:g.49158680_49158682delinsCAG	NCBI36
NG_008920.1:g.6442_6444delinsCAG
NG_033054.1:g.3418_3420delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305386.4:c.944_946delinsCAG MANE Select	ENSP00000307423.2:p.Thr315=
ENST00000305386.3:c.944_946delinsCAG	ENSP00000307423.2:p.Thr315=
NM_002408.3:c.944_946delinsCAG	NP_002399.1:p.Thr315=
NM_002408.4:c.944_946delinsCAG MANE Select	NP_002399.1:p.Thr315=