Canonical Allele Identifier: CA2683855111
Gene: LMTK2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98187061_98187062insAA , CM000669.2:g.98187061_98187062insAA GRCh38
NC_000007.13:g.97816373_97816374insAA , CM000669.1:g.97816373_97816374insAA GRCh37
NC_000007.12:g.97654309_97654310insAA NCBI36
NG_013375.1:g.85177_85178insAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.998+63_998+64insAA MANE Select ENSP00000297293.5:n.998+63_998+64insAA
ENST00000297293.5:c.998+63_998+64insAA ENSP00000297293.5:n.998+63_998+64insAA
NM_014916.3:c.998+63_998+64insAA NP_055731.2:n.998+63_998+64insAA
XM_011515981.1:c.992+63_992+64insAA XP_011514283.1:n.992+63_992+64insAA
XM_011515981.3:c.992+63_992+64insAA XP_011514283.1:n.992+63_992+64insAA
NM_014916.4:c.998+63_998+64insAA MANE Select NP_055731.2:n.998+63_998+64insAA