Canonical Allele Identifier: CA368269964

Gene: LMTK2

Linked Data

• MyVariant Identifiers: chr7:g.97816253T>A (hg19) ; chr7:g.98186941T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.98186941T>A , CM000669.2:g.98186941T>A	GRCh38
NC_000007.13:g.97816253T>A , CM000669.1:g.97816253T>A	GRCh37
NC_000007.12:g.97654189T>A	NCBI36
NG_013375.1:g.85057T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297293.6:c.941T>A MANE Select	ENSP00000297293.5:p.Val314Glu
ENST00000297293.5:c.941T>A	ENSP00000297293.5:p.Val314Glu
NM_014916.3:c.941T>A	NP_055731.2:p.Val314Glu
XM_011515981.1:c.935T>A	XP_011514283.1:p.Val312Glu
XM_011515981.3:c.935T>A	XP_011514283.1:p.Val312Glu
NM_014916.4:c.941T>A MANE Select	NP_055731.2:p.Val314Glu