Canonical Allele Identifier: CA1728472089
Gene: LMTK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98186826C= , CM000669.2:g.98186826C= GRCh38
NC_000007.13:g.97816138C= , CM000669.1:g.97816138C= GRCh37
NC_000007.12:g.97654074C= NCBI36
NG_013375.1:g.84942C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.877-51C= MANE Select ENSP00000297293.5:n.877-51C=
ENST00000297293.5:c.877-51C= ENSP00000297293.5:n.877-51C=
NM_014916.3:c.877-51C= NP_055731.2:n.877-51C=
XM_011515981.1:c.871-51C= XP_011514283.1:n.871-51C=
XM_011515981.3:c.871-51C= XP_011514283.1:n.871-51C=
NM_014916.4:c.877-51C= MANE Select NP_055731.2:n.877-51C=