Canonical Allele Identifier: CA368270174

Gene: LMTK2

Linked Data

• MyVariant Identifiers: chr7:g.97816291A>T (hg19) ; chr7:g.98186979A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.98186979A>T , CM000669.2:g.98186979A>T	GRCh38
NC_000007.13:g.97816291A>T , CM000669.1:g.97816291A>T	GRCh37
NC_000007.12:g.97654227A>T	NCBI36
NG_013375.1:g.85095A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297293.6:c.979A>T MANE Select	ENSP00000297293.5:p.Thr327Ser
ENST00000297293.5:c.979A>T	ENSP00000297293.5:p.Thr327Ser
NM_014916.3:c.979A>T	NP_055731.2:p.Thr327Ser
XM_011515981.1:c.973A>T	XP_011514283.1:p.Thr325Ser
XM_011515981.3:c.973A>T	XP_011514283.1:p.Thr325Ser
NM_014916.4:c.979A>T MANE Select	NP_055731.2:p.Thr327Ser