Canonical Allele Identifier: CA51723704
Gene: MAT2A HGNC NCBI

Linked Data

dbSNP Id: rs902505983
MyVariant Identifiers: chr2:g.85767649_85767654del (hg19) chr2:g.85540526_85540531del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85540529_85540534del , CM000664.2:g.85540529_85540534del GRCh38
NC_000002.11:g.85767652_85767657del , CM000664.1:g.85767652_85767657del GRCh37
NC_000002.10:g.85621163_85621168del NCBI36
NG_029183.1:g.6552_6557del

Transcript Alleles

HGVS Amino-acid Change
ENST00000306434.8:c.92-554_92-549del MANE Select ENSP00000303147.3:n.92-554_92-549del
ENST00000306434.7:c.92-554_92-549del ENSP00000303147.3:n.92-554_92-549del
ENST00000409017.1:c.-99+529_-99+534del ENSP00000386353.1:n.-99+529_-99+534del
ENST00000465151.5:n.212-554_212-549del
ENST00000469221.5:n.212-554_212-549del
ENST00000481412.5:n.70-554_70-549del
NM_005911.5:c.92-554_92-549del NP_005902.1:n.92-554_92-549del
NM_005911.6:c.92-554_92-549del MANE Select NP_005902.1:n.92-554_92-549del
Search 100 bp 5'
Search 100 bp 3'