Canonical Allele Identifier: CA368270097

Gene: LMTK2

Linked Data

• MyVariant Identifiers: chr7:g.97816283C>T (hg19) ; chr7:g.98186971C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.98186971C>T , CM000669.2:g.98186971C>T	GRCh38
NC_000007.13:g.97816283C>T , CM000669.1:g.97816283C>T	GRCh37
NC_000007.12:g.97654219C>T	NCBI36
NG_013375.1:g.85087C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297293.6:c.971C>T MANE Select	ENSP00000297293.5:p.Ala324Val
ENST00000297293.5:c.971C>T	ENSP00000297293.5:p.Ala324Val
NM_014916.3:c.971C>T	NP_055731.2:p.Ala324Val
XM_011515981.1:c.965C>T	XP_011514283.1:p.Ala322Val
XM_011515981.3:c.965C>T	XP_011514283.1:p.Ala322Val
NM_014916.4:c.971C>T MANE Select	NP_055731.2:p.Ala324Val