Canonical Allele Identifier: CA1728472279

Gene: LMTK2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.98187319_98187321delinsCTG , CM000669.2:g.98187319_98187321delinsCTG	GRCh38
NC_000007.13:g.97816631_97816633delinsCTG , CM000669.1:g.97816631_97816633delinsCTG	GRCh37
NC_000007.12:g.97654567_97654569delinsCTG	NCBI36
NG_013375.1:g.85435_85437delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297293.6:c.998+321_998+323delinsCTG MANE Select	ENSP00000297293.5:n.998+321_998+323delinsCTG
ENST00000297293.5:c.998+321_998+323delinsCTG	ENSP00000297293.5:n.998+321_998+323delinsCTG
NM_014916.3:c.998+321_998+323delinsCTG	NP_055731.2:n.998+321_998+323delinsCTG
XM_011515981.1:c.992+321_992+323delinsCTG	XP_011514283.1:n.992+321_992+323delinsCTG
XM_011515981.3:c.992+321_992+323delinsCTG	XP_011514283.1:n.992+321_992+323delinsCTG
NM_014916.4:c.998+321_998+323delinsCTG MANE Select	NP_055731.2:n.998+321_998+323delinsCTG