Canonical Allele Identifier: CA2578947384
Gene: LMTK2 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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