Canonical Allele Identifier: CA2777082555
Gene: LMTK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98187179G>T , CM000669.2:g.98187179G>T GRCh38
NC_000007.13:g.97816491G>T , CM000669.1:g.97816491G>T GRCh37
NC_000007.12:g.97654427G>T NCBI36
NG_013375.1:g.85295G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.998+181G>T MANE Select ENSP00000297293.5:n.998+181G>T
ENST00000297293.5:c.998+181G>T ENSP00000297293.5:n.998+181G>T
NM_014916.3:c.998+181G>T NP_055731.2:n.998+181G>T
XM_011515981.1:c.992+181G>T XP_011514283.1:n.992+181G>T
XM_011515981.3:c.992+181G>T XP_011514283.1:n.992+181G>T
NM_014916.4:c.998+181G>T MANE Select NP_055731.2:n.998+181G>T