Canonical Allele Identifier: CA1728472256
Gene: LMTK2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98187257C= , CM000669.2:g.98187257C= GRCh38
NC_000007.13:g.97816569C= , CM000669.1:g.97816569C= GRCh37
NC_000007.12:g.97654505C= NCBI36
NG_013375.1:g.85373C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.998+259C= MANE Select ENSP00000297293.5:n.998+259C=
ENST00000297293.5:c.998+259C= ENSP00000297293.5:n.998+259C=
NM_014916.3:c.998+259C= NP_055731.2:n.998+259C=
XM_011515981.1:c.992+259C= XP_011514283.1:n.992+259C=
XM_011515981.3:c.992+259C= XP_011514283.1:n.992+259C=
NM_014916.4:c.998+259C= MANE Select NP_055731.2:n.998+259C=
Search 100 bp 5'
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