Canonical Allele Identifier: CA1728472165
Gene: LMTK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98187052C= , CM000669.2:g.98187052C= GRCh38
NC_000007.13:g.97816364C= , CM000669.1:g.97816364C= GRCh37
NC_000007.12:g.97654300C= NCBI36
NG_013375.1:g.85168C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.998+54C= MANE Select ENSP00000297293.5:n.998+54C=
ENST00000297293.5:c.998+54C= ENSP00000297293.5:n.998+54C=
NM_014916.3:c.998+54C= NP_055731.2:n.998+54C=
XM_011515981.1:c.992+54C= XP_011514283.1:n.992+54C=
XM_011515981.3:c.992+54C= XP_011514283.1:n.992+54C=
NM_014916.4:c.998+54C= MANE Select NP_055731.2:n.998+54C=