Canonical Allele Identifier: CA368270177
Gene: LMTK2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.97816291A>G (hg19) chr7:g.98186979A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98186979A>G , CM000669.2:g.98186979A>G GRCh38
NC_000007.13:g.97816291A>G , CM000669.1:g.97816291A>G GRCh37
NC_000007.12:g.97654227A>G NCBI36
NG_013375.1:g.85095A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.979A>G MANE Select ENSP00000297293.5:p.Thr327Ala
ENST00000297293.5:c.979A>G ENSP00000297293.5:p.Thr327Ala
NM_014916.3:c.979A>G NP_055731.2:p.Thr327Ala
XM_011515981.1:c.973A>G XP_011514283.1:p.Thr325Ala
XM_011515981.3:c.973A>G XP_011514283.1:p.Thr325Ala
NM_014916.4:c.979A>G MANE Select NP_055731.2:p.Thr327Ala
Search 100 bp 5'
Search 100 bp 3'