Canonical Allele Identifier: CA1266821830
Gene: MAT2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85540525_85540531delinsCGAACTT , CM000664.2:g.85540525_85540531delinsCGAACTT GRCh38
NC_000002.11:g.85767648_85767654delinsCGAACTT , CM000664.1:g.85767648_85767654delinsCGAACTT GRCh37
NC_000002.10:g.85621159_85621165delinsCGAACTT NCBI36
NG_029183.1:g.6548_6554delinsCGAACTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000306434.8:c.92-558_92-552delinsCGAACTT MANE Select ENSP00000303147.3:n.92-558_92-552delinsCGAACTT
ENST00000306434.7:c.92-558_92-552delinsCGAACTT ENSP00000303147.3:n.92-558_92-552delinsCGAACTT
ENST00000409017.1:c.-99+525_-99+531delinsCGAACTT ENSP00000386353.1:n.-99+525_-99+531delinsCGAACTT
ENST00000465151.5:n.212-558_212-552delinsCGAACTT
ENST00000469221.5:n.212-558_212-552delinsCGAACTT
ENST00000481412.5:n.70-558_70-552delinsCGAACTT
NM_005911.5:c.92-558_92-552delinsCGAACTT NP_005902.1:n.92-558_92-552delinsCGAACTT
NM_005911.6:c.92-558_92-552delinsCGAACTT MANE Select NP_005902.1:n.92-558_92-552delinsCGAACTT