Canonical Allele Identifier: CA1728472199
Gene: LMTK2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98187114T= , CM000669.2:g.98187114T= GRCh38
NC_000007.13:g.97816426T= , CM000669.1:g.97816426T= GRCh37
NC_000007.12:g.97654362T= NCBI36
NG_013375.1:g.85230T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.998+116T= MANE Select ENSP00000297293.5:n.998+116T=
ENST00000297293.5:c.998+116T= ENSP00000297293.5:n.998+116T=
NM_014916.3:c.998+116T= NP_055731.2:n.998+116T=
XM_011515981.1:c.992+116T= XP_011514283.1:n.992+116T=
XM_011515981.3:c.992+116T= XP_011514283.1:n.992+116T=
NM_014916.4:c.998+116T= MANE Select NP_055731.2:n.998+116T=
Search 100 bp 5'
Search 100 bp 3'