Canonical Allele Identifier: CA368269717
Gene: LMTK2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.97816190A>C (hg19) chr7:g.98186878A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98186878A>C , CM000669.2:g.98186878A>C GRCh38
NC_000007.13:g.97816190A>C , CM000669.1:g.97816190A>C GRCh37
NC_000007.12:g.97654126A>C NCBI36
NG_013375.1:g.84994A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.878A>C MANE Select ENSP00000297293.5:p.Glu293Ala
ENST00000297293.5:c.878A>C ENSP00000297293.5:p.Glu293Ala
NM_014916.3:c.878A>C NP_055731.2:p.Glu293Ala
XM_011515981.1:c.872A>C XP_011514283.1:p.Glu291Ala
XM_011515981.3:c.872A>C XP_011514283.1:p.Glu291Ala
NM_014916.4:c.878A>C MANE Select NP_055731.2:p.Glu293Ala
Search 100 bp 5'
Search 100 bp 3'