Canonical Allele Identifier: CA342814918

Gene: LAMTOR2

Linked Data

• MyVariant Identifiers: chr1:g.156025110C>A (hg19) ; chr1:g.156055319C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156055319C>A , CM000663.2:g.156055319C>A	GRCh38
NC_000001.10:g.156025110C>A , CM000663.1:g.156025110C>A	GRCh37
NC_000001.9:g.154291734C>A	NCBI36
NG_009898.1:g.5594C>A , LRG_81:g.5594C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000368305.9:c.125C>A MANE Select	ENSP00000357288.4:p.Ala42Asp
ENST00000368302.3:c.125C>A	ENSP00000357285.3:p.Ala42Asp
ENST00000368304.9:c.125C>A	ENSP00000357287.5:p.Ala42Asp
ENST00000368305.8:c.125C>A	ENSP00000357288.4:p.Ala42Asp
ENST00000487106.5:n.235C>A
ENST00000489664.1:n.194C>A
NM_001145264.1:c.125C>A	NP_001138736.1:p.Ala42Asp
NM_014017.3:c.125C>A , LRG_81t1:c.125C>A	NP_054736.1:p.Ala42Asp
NM_001145264.2:c.125C>A	NP_001138736.1:p.Ala42Asp
NM_014017.4:c.125C>A MANE Select	NP_054736.1:p.Ala42Asp