Canonical Allele Identifier: CA368269756

Gene: LMTK2

Linked Data

• MyVariant Identifiers: chr7:g.97816199T>G (hg19) ; chr7:g.98186887T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.98186887T>G , CM000669.2:g.98186887T>G	GRCh38
NC_000007.13:g.97816199T>G , CM000669.1:g.97816199T>G	GRCh37
NC_000007.12:g.97654135T>G	NCBI36
NG_013375.1:g.85003T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297293.6:c.887T>G MANE Select	ENSP00000297293.5:p.Ile296Ser
ENST00000297293.5:c.887T>G	ENSP00000297293.5:p.Ile296Ser
NM_014916.3:c.887T>G	NP_055731.2:p.Ile296Ser
XM_011515981.1:c.881T>G	XP_011514283.1:p.Ile294Ser
XM_011515981.3:c.881T>G	XP_011514283.1:p.Ile294Ser
NM_014916.4:c.887T>G MANE Select	NP_055731.2:p.Ile296Ser