Canonical Allele Identifier: CA1728472090
Gene: LMTK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98186828C= , CM000669.2:g.98186828C= GRCh38
NC_000007.13:g.97816140C= , CM000669.1:g.97816140C= GRCh37
NC_000007.12:g.97654076C= NCBI36
NG_013375.1:g.84944C=

Transcript Alleles

HGVS Amino-acid change
ENST00000297293.6:c.877-49C= MANE Select ENSP00000297293.5:n.877-49C=
ENST00000297293.5:c.877-49C= ENSP00000297293.5:n.877-49C=
NM_014916.3:c.877-49C= NP_055731.2:n.877-49C=
XM_011515981.1:c.871-49C= XP_011514283.1:n.871-49C=
XM_011515981.3:c.871-49C= XP_011514283.1:n.871-49C=
NM_014916.4:c.877-49C= MANE Select NP_055731.2:n.877-49C=