Canonical Allele Identifier: CA1266821838
Gene: MAT2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85540532_85540533delinsGA , CM000664.2:g.85540532_85540533delinsGA GRCh38
NC_000002.11:g.85767655_85767656delinsGA , CM000664.1:g.85767655_85767656delinsGA GRCh37
NC_000002.10:g.85621166_85621167delinsGA NCBI36
NG_029183.1:g.6555_6556delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000306434.8:c.92-551_92-550delinsGA MANE Select ENSP00000303147.3:n.92-551_92-550delinsGA
ENST00000306434.7:c.92-551_92-550delinsGA ENSP00000303147.3:n.92-551_92-550delinsGA
ENST00000409017.1:c.-99+532_-99+533delinsGA ENSP00000386353.1:n.-99+532_-99+533delinsGA
ENST00000465151.5:n.212-551_212-550delinsGA
ENST00000469221.5:n.212-551_212-550delinsGA
ENST00000481412.5:n.70-551_70-550delinsGA
NM_005911.5:c.92-551_92-550delinsGA NP_005902.1:n.92-551_92-550delinsGA
NM_005911.6:c.92-551_92-550delinsGA MANE Select NP_005902.1:n.92-551_92-550delinsGA