Canonical Allele Identifier: CA421067874

Gene: LAMTOR2

Linked Data

• gnomAD v4: 1-156055317-C-T
• MyVariant Identifiers: chr1:g.156025108C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156055317C>T , CM000663.2:g.156055317C>T	GRCh38
NC_000001.10:g.156025108C>T , CM000663.1:g.156025108C>T	GRCh37
NC_000001.9:g.154291732C>T	NCBI36
NG_009898.1:g.5592C>T , LRG_81:g.5592C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000368305.9:c.123C>T MANE Select	ENSP00000357288.4:p.Asp41=
ENST00000368302.3:c.123C>T	ENSP00000357285.3:p.Asp41=
ENST00000368304.9:c.123C>T	ENSP00000357287.5:p.Asp41=
ENST00000368305.8:c.123C>T	ENSP00000357288.4:p.Asp41=
ENST00000487106.5:n.233C>T
ENST00000489664.1:n.192C>T
NM_001145264.1:c.123C>T	NP_001138736.1:p.Asp41=
NM_014017.3:c.123C>T , LRG_81t1:c.123C>T	NP_054736.1:p.Asp41=
NM_001145264.2:c.123C>T	NP_001138736.1:p.Asp41=
NM_014017.4:c.123C>T MANE Select	NP_054736.1:p.Asp41=