Canonical Allele Identifier: CA368269913
Gene: LMTK2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.97816241C>A (hg19) chr7:g.98186929C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98186929C>A , CM000669.2:g.98186929C>A GRCh38
NC_000007.13:g.97816241C>A , CM000669.1:g.97816241C>A GRCh37
NC_000007.12:g.97654177C>A NCBI36
NG_013375.1:g.85045C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.929C>A MANE Select ENSP00000297293.5:p.Ala310Asp
ENST00000297293.5:c.929C>A ENSP00000297293.5:p.Ala310Asp
NM_014916.3:c.929C>A NP_055731.2:p.Ala310Asp
XM_011515981.1:c.923C>A XP_011514283.1:p.Ala308Asp
XM_011515981.3:c.923C>A XP_011514283.1:p.Ala308Asp
NM_014916.4:c.929C>A MANE Select NP_055731.2:p.Ala310Asp
Search 100 bp 5'
Search 100 bp 3'