Canonical Allele Identifier: CA1266821952
Gene: MAT2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85540633_85540634delinsGT , CM000664.2:g.85540633_85540634delinsGT GRCh38
NC_000002.11:g.85767756_85767757delinsGT , CM000664.1:g.85767756_85767757delinsGT GRCh37
NC_000002.10:g.85621267_85621268delinsGT NCBI36
NG_029183.1:g.6656_6657delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000306434.8:c.92-450_92-449delinsGT MANE Select ENSP00000303147.3:n.92-450_92-449delinsGT
ENST00000306434.7:c.92-450_92-449delinsGT ENSP00000303147.3:n.92-450_92-449delinsGT
ENST00000409017.1:c.-98-450_-98-449delinsGT ENSP00000386353.1:n.-98-450_-98-449delinsGT
ENST00000465151.5:n.212-450_212-449delinsGT
ENST00000469221.5:n.212-450_212-449delinsGT
ENST00000481412.5:n.70-450_70-449delinsGT
NM_005911.5:c.92-450_92-449delinsGT NP_005902.1:n.92-450_92-449delinsGT
NM_005911.6:c.92-450_92-449delinsGT MANE Select NP_005902.1:n.92-450_92-449delinsGT