Canonical Allele Identifier: CA368269760
Gene: LMTK2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.97816201G>A (hg19) chr7:g.98186889G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98186889G>A , CM000669.2:g.98186889G>A GRCh38
NC_000007.13:g.97816201G>A , CM000669.1:g.97816201G>A GRCh37
NC_000007.12:g.97654137G>A NCBI36
NG_013375.1:g.85005G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.889G>A MANE Select ENSP00000297293.5:p.Glu297Lys
ENST00000297293.5:c.889G>A ENSP00000297293.5:p.Glu297Lys
NM_014916.3:c.889G>A NP_055731.2:p.Glu297Lys
XM_011515981.1:c.883G>A XP_011514283.1:p.Glu295Lys
XM_011515981.3:c.883G>A XP_011514283.1:p.Glu295Lys
NM_014916.4:c.889G>A MANE Select NP_055731.2:p.Glu297Lys
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