Canonical Allele Identifier: CA1154316
Gene: LAMTOR2 HGNC NCBI

Linked Data

dbSNP Id: rs779532617

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156055308G>A , CM000663.2:g.156055308G>A GRCh38
NC_000001.10:g.156025099G>A , CM000663.1:g.156025099G>A GRCh37
NC_000001.9:g.154291723G>A NCBI36
NG_009898.1:g.5583G>A , LRG_81:g.5583G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000368305.9:c.114G>A MANE Select ENSP00000357288.4:p.Gly38=
ENST00000368302.3:c.114G>A ENSP00000357285.3:p.Gly38=
ENST00000368304.9:c.114G>A ENSP00000357287.5:p.Gly38=
ENST00000368305.8:c.114G>A ENSP00000357288.4:p.Gly38=
ENST00000487106.5:n.224G>A
ENST00000489664.1:n.183G>A
NM_001145264.1:c.114G>A NP_001138736.1:p.Gly38=
NM_014017.3:c.114G>A , LRG_81t1:c.114G>A NP_054736.1:p.Gly38=
NM_001145264.2:c.114G>A NP_001138736.1:p.Gly38=
NM_014017.4:c.114G>A MANE Select NP_054736.1:p.Gly38=