Canonical Allele Identifier: CA368270167

Gene: LMTK2

Linked Data

• COSMIC: COSM1187367 ; COSM1187368
• MyVariant Identifiers: chr7:g.97816290G>T (hg19) ; chr7:g.98186978G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.98186978G>T , CM000669.2:g.98186978G>T	GRCh38
NC_000007.13:g.97816290G>T , CM000669.1:g.97816290G>T	GRCh37
NC_000007.12:g.97654226G>T	NCBI36
NG_013375.1:g.85094G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297293.6:c.978G>T MANE Select	ENSP00000297293.5:p.Gln326His
ENST00000297293.5:c.978G>T	ENSP00000297293.5:p.Gln326His
NM_014916.3:c.978G>T	NP_055731.2:p.Gln326His
XM_011515981.1:c.972G>T	XP_011514283.1:p.Gln324His
XM_011515981.3:c.972G>T	XP_011514283.1:p.Gln324His
NM_014916.4:c.978G>T MANE Select	NP_055731.2:p.Gln326His