Canonical Allele Identifier: CA1728472218
Gene: LMTK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98187167_98187170delinsTGTG , CM000669.2:g.98187167_98187170delinsTGTG GRCh38
NC_000007.13:g.97816479_97816482delinsTGTG , CM000669.1:g.97816479_97816482delinsTGTG GRCh37
NC_000007.12:g.97654415_97654418delinsTGTG NCBI36
NG_013375.1:g.85283_85286delinsTGTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.998+169_998+172delinsTGTG MANE Select ENSP00000297293.5:n.998+169_998+172delinsTGTG
ENST00000297293.5:c.998+169_998+172delinsTGTG ENSP00000297293.5:n.998+169_998+172delinsTGTG
NM_014916.3:c.998+169_998+172delinsTGTG NP_055731.2:n.998+169_998+172delinsTGTG
XM_011515981.1:c.992+169_992+172delinsTGTG XP_011514283.1:n.992+169_992+172delinsTGTG
XM_011515981.3:c.992+169_992+172delinsTGTG XP_011514283.1:n.992+169_992+172delinsTGTG
NM_014916.4:c.998+169_998+172delinsTGTG MANE Select NP_055731.2:n.998+169_998+172delinsTGTG