Canonical Allele Identifier: CA918081464

Gene: LMTK2

Linked Data

• dbSNP Id: rs1562918638

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.98187063_98187064insC , CM000669.2:g.98187063_98187064insC	GRCh38
NC_000007.13:g.97816375_97816376insC , CM000669.1:g.97816375_97816376insC	GRCh37
NC_000007.12:g.97654311_97654312insC	NCBI36
NG_013375.1:g.85179_85180insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297293.6:c.998+65_998+66insC MANE Select	ENSP00000297293.5:n.998+65_998+66insC
ENST00000297293.5:c.998+65_998+66insC	ENSP00000297293.5:n.998+65_998+66insC
NM_014916.3:c.998+65_998+66insC	NP_055731.2:n.998+65_998+66insC
XM_011515981.1:c.992+65_992+66insC	XP_011514283.1:n.992+65_992+66insC
XM_011515981.3:c.992+65_992+66insC	XP_011514283.1:n.992+65_992+66insC
NM_014916.4:c.998+65_998+66insC MANE Select	NP_055731.2:n.998+65_998+66insC