Canonical Allele Identifier: CA1728472178
Gene: LMTK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98187073_98187078delinsTAAAGG , CM000669.2:g.98187073_98187078delinsTAAAGG GRCh38
NC_000007.13:g.97816385_97816390delinsTAAAGG , CM000669.1:g.97816385_97816390delinsTAAAGG GRCh37
NC_000007.12:g.97654321_97654326delinsTAAAGG NCBI36
NG_013375.1:g.85189_85194delinsTAAAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.998+75_998+80delinsTAAAGG MANE Select ENSP00000297293.5:n.998+75_998+80delinsTAAAGG
ENST00000297293.5:c.998+75_998+80delinsTAAAGG ENSP00000297293.5:n.998+75_998+80delinsTAAAGG
NM_014916.3:c.998+75_998+80delinsTAAAGG NP_055731.2:n.998+75_998+80delinsTAAAGG
XM_011515981.1:c.992+75_992+80delinsTAAAGG XP_011514283.1:n.992+75_992+80delinsTAAAGG
XM_011515981.3:c.992+75_992+80delinsTAAAGG XP_011514283.1:n.992+75_992+80delinsTAAAGG
NM_014916.4:c.998+75_998+80delinsTAAAGG MANE Select NP_055731.2:n.998+75_998+80delinsTAAAGG