Canonical Allele Identifier: CA1266821870
Gene: MAT2A HGNC NCBI

Linked Data

dbSNP Id: rs1691448862
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85540558_85540560del , CM000664.2:g.85540558_85540560del GRCh38
NC_000002.11:g.85767681_85767683del , CM000664.1:g.85767681_85767683del GRCh37
NC_000002.10:g.85621192_85621194del NCBI36
NG_029183.1:g.6581_6583del

Transcript Alleles

HGVS Amino-acid Change
ENST00000306434.8:c.92-525_92-523del MANE Select ENSP00000303147.3:n.92-525_92-523del
ENST00000306434.7:c.92-525_92-523del ENSP00000303147.3:n.92-525_92-523del
ENST00000409017.1:c.-98-525_-98-523del ENSP00000386353.1:n.-98-525_-98-523del
ENST00000465151.5:n.212-525_212-523del
ENST00000469221.5:n.212-525_212-523del
ENST00000481412.5:n.70-525_70-523del
NM_005911.5:c.92-525_92-523del NP_005902.1:n.92-525_92-523del
NM_005911.6:c.92-525_92-523del MANE Select NP_005902.1:n.92-525_92-523del
Search 100 bp 5'
Search 100 bp 3'