Canonical Allele Identifier: CA1728472217
Gene: LMTK2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98187167T= , CM000669.2:g.98187167T= GRCh38
NC_000007.13:g.97816479T= , CM000669.1:g.97816479T= GRCh37
NC_000007.12:g.97654415T= NCBI36
NG_013375.1:g.85283T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.998+169T= MANE Select ENSP00000297293.5:n.998+169T=
ENST00000297293.5:c.998+169T= ENSP00000297293.5:n.998+169T=
NM_014916.3:c.998+169T= NP_055731.2:n.998+169T=
XM_011515981.1:c.992+169T= XP_011514283.1:n.992+169T=
XM_011515981.3:c.992+169T= XP_011514283.1:n.992+169T=
NM_014916.4:c.998+169T= MANE Select NP_055731.2:n.998+169T=
Search 100 bp 5'
Search 100 bp 3'