Canonical Allele Identifier: CA368269935

Gene: LMTK2

Linked Data

• MyVariant Identifiers: chr7:g.97816247A>T (hg19) ; chr7:g.98186935A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.98186935A>T , CM000669.2:g.98186935A>T	GRCh38
NC_000007.13:g.97816247A>T , CM000669.1:g.97816247A>T	GRCh37
NC_000007.12:g.97654183A>T	NCBI36
NG_013375.1:g.85051A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297293.6:c.935A>T MANE Select	ENSP00000297293.5:p.Glu312Val
ENST00000297293.5:c.935A>T	ENSP00000297293.5:p.Glu312Val
NM_014916.3:c.935A>T	NP_055731.2:p.Glu312Val
XM_011515981.1:c.929A>T	XP_011514283.1:p.Glu310Val
XM_011515981.3:c.929A>T	XP_011514283.1:p.Glu310Val
NM_014916.4:c.935A>T MANE Select	NP_055731.2:p.Glu312Val