Canonical Allele Identifier: CA368269900

Gene: LMTK2

Linked Data

• MyVariant Identifiers: chr7:g.97816237A>T (hg19) ; chr7:g.98186925A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.98186925A>T , CM000669.2:g.98186925A>T	GRCh38
NC_000007.13:g.97816237A>T , CM000669.1:g.97816237A>T	GRCh37
NC_000007.12:g.97654173A>T	NCBI36
NG_013375.1:g.85041A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297293.6:c.925A>T MANE Select	ENSP00000297293.5:p.Thr309Ser
ENST00000297293.5:c.925A>T	ENSP00000297293.5:p.Thr309Ser
NM_014916.3:c.925A>T	NP_055731.2:p.Thr309Ser
XM_011515981.1:c.919A>T	XP_011514283.1:p.Thr307Ser
XM_011515981.3:c.919A>T	XP_011514283.1:p.Thr307Ser
NM_014916.4:c.925A>T MANE Select	NP_055731.2:p.Thr309Ser