Canonical Allele Identifier: CA2578947388
Gene: LMTK2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98187089_98187096del , CM000669.2:g.98187089_98187096del GRCh38
NC_000007.13:g.97816401_97816408del , CM000669.1:g.97816401_97816408del GRCh37
NC_000007.12:g.97654337_97654344del NCBI36
NG_013375.1:g.85205_85212del

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.998+91_998+98del MANE Select ENSP00000297293.5:n.998+91_998+98del
ENST00000297293.5:c.998+91_998+98del ENSP00000297293.5:n.998+91_998+98del
NM_014916.3:c.998+91_998+98del NP_055731.2:n.998+91_998+98del
XM_011515981.1:c.992+91_992+98del XP_011514283.1:n.992+91_992+98del
XM_011515981.3:c.992+91_992+98del XP_011514283.1:n.992+91_992+98del
NM_014916.4:c.998+91_998+98del MANE Select NP_055731.2:n.998+91_998+98del