Canonical Allele Identifier: CA2683855169
Gene: LMTK2 HGNC NCBI

Linked Data

gnomAD v4: 7-98187145-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98187145C>A , CM000669.2:g.98187145C>A GRCh38
NC_000007.13:g.97816457C>A , CM000669.1:g.97816457C>A GRCh37
NC_000007.12:g.97654393C>A NCBI36
NG_013375.1:g.85261C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.998+147C>A MANE Select ENSP00000297293.5:n.998+147C>A
ENST00000297293.5:c.998+147C>A ENSP00000297293.5:n.998+147C>A
NM_014916.3:c.998+147C>A NP_055731.2:n.998+147C>A
XM_011515981.1:c.992+147C>A XP_011514283.1:n.992+147C>A
XM_011515981.3:c.992+147C>A XP_011514283.1:n.992+147C>A
NM_014916.4:c.998+147C>A MANE Select NP_055731.2:n.998+147C>A
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