Canonical Allele Identifier: CA2683855070
Gene: LMTK2 HGNC NCBI

Linked Data

gnomAD v4: 7-98187009-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98187009G>T , CM000669.2:g.98187009G>T GRCh38
NC_000007.13:g.97816321G>T , CM000669.1:g.97816321G>T GRCh37
NC_000007.12:g.97654257G>T NCBI36
NG_013375.1:g.85125G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.998+11G>T MANE Select ENSP00000297293.5:n.998+11G>T
ENST00000297293.5:c.998+11G>T ENSP00000297293.5:n.998+11G>T
NM_014916.3:c.998+11G>T NP_055731.2:n.998+11G>T
XM_011515981.1:c.992+11G>T XP_011514283.1:n.992+11G>T
XM_011515981.3:c.992+11G>T XP_011514283.1:n.992+11G>T
NM_014916.4:c.998+11G>T MANE Select NP_055731.2:n.998+11G>T