Canonical Allele Identifier: CA1728472105
Gene: LMTK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98186857T= , CM000669.2:g.98186857T= GRCh38
NC_000007.13:g.97816169T= , CM000669.1:g.97816169T= GRCh37
NC_000007.12:g.97654105T= NCBI36
NG_013375.1:g.84973T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.877-20T= MANE Select ENSP00000297293.5:n.877-20T=
ENST00000297293.5:c.877-20T= ENSP00000297293.5:n.877-20T=
NM_014916.3:c.877-20T= NP_055731.2:n.877-20T=
XM_011515981.1:c.871-20T= XP_011514283.1:n.871-20T=
XM_011515981.3:c.871-20T= XP_011514283.1:n.871-20T=
NM_014916.4:c.877-20T= MANE Select NP_055731.2:n.877-20T=