Canonical Allele Identifier: CA1266821945
Gene: MAT2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85540628_85540630delinsCTT , CM000664.2:g.85540628_85540630delinsCTT GRCh38
NC_000002.11:g.85767751_85767753delinsCTT , CM000664.1:g.85767751_85767753delinsCTT GRCh37
NC_000002.10:g.85621262_85621264delinsCTT NCBI36
NG_029183.1:g.6651_6653delinsCTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000306434.8:c.92-455_92-453delinsCTT MANE Select ENSP00000303147.3:n.92-455_92-453delinsCTT
ENST00000306434.7:c.92-455_92-453delinsCTT ENSP00000303147.3:n.92-455_92-453delinsCTT
ENST00000409017.1:c.-98-455_-98-453delinsCTT ENSP00000386353.1:n.-98-455_-98-453delinsCTT
ENST00000465151.5:n.212-455_212-453delinsCTT
ENST00000469221.5:n.212-455_212-453delinsCTT
ENST00000481412.5:n.70-455_70-453delinsCTT
NM_005911.5:c.92-455_92-453delinsCTT NP_005902.1:n.92-455_92-453delinsCTT
NM_005911.6:c.92-455_92-453delinsCTT MANE Select NP_005902.1:n.92-455_92-453delinsCTT