Canonical Allele Identifier: CA1728472257
Gene: LMTK2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98187259C= , CM000669.2:g.98187259C= GRCh38
NC_000007.13:g.97816571C= , CM000669.1:g.97816571C= GRCh37
NC_000007.12:g.97654507C= NCBI36
NG_013375.1:g.85375C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.998+261C= MANE Select ENSP00000297293.5:n.998+261C=
ENST00000297293.5:c.998+261C= ENSP00000297293.5:n.998+261C=
NM_014916.3:c.998+261C= NP_055731.2:n.998+261C=
XM_011515981.1:c.992+261C= XP_011514283.1:n.992+261C=
XM_011515981.3:c.992+261C= XP_011514283.1:n.992+261C=
NM_014916.4:c.998+261C= MANE Select NP_055731.2:n.998+261C=
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