Canonical Allele Identifier: CA1104852620
Gene: LMTK2 HGNC NCBI

Linked Data

dbSNP Id: rs1797446934
gnomAD v3: 7-98187065-T-TCAA
gnomAD v4: 7-98187065-T-TCAA
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98187065_98187066insCAA , CM000669.2:g.98187065_98187066insCAA GRCh38
NC_000007.13:g.97816377_97816378insCAA , CM000669.1:g.97816377_97816378insCAA GRCh37
NC_000007.12:g.97654313_97654314insCAA NCBI36
NG_013375.1:g.85181_85182insCAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.998+67_998+68insCAA MANE Select ENSP00000297293.5:n.998+67_998+68insCAA
ENST00000297293.5:c.998+67_998+68insCAA ENSP00000297293.5:n.998+67_998+68insCAA
NM_014916.3:c.998+67_998+68insCAA NP_055731.2:n.998+67_998+68insCAA
XM_011515981.1:c.992+67_992+68insCAA XP_011514283.1:n.992+67_992+68insCAA
XM_011515981.3:c.992+67_992+68insCAA XP_011514283.1:n.992+67_992+68insCAA
NM_014916.4:c.998+67_998+68insCAA MANE Select NP_055731.2:n.998+67_998+68insCAA
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