Canonical Allele Identifier: CA4355295
Gene: LMTK2 HGNC NCBI

Linked Data

dbSNP Id: rs778347846

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98186836_98186840del , CM000669.2:g.98186836_98186840del GRCh38
NC_000007.13:g.97816148_97816152del , CM000669.1:g.97816148_97816152del GRCh37
NC_000007.12:g.97654084_97654088del NCBI36
NG_013375.1:g.84952_84956del

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.877-41_877-37del MANE Select ENSP00000297293.5:n.877-41_877-37del
ENST00000297293.5:c.877-41_877-37del ENSP00000297293.5:n.877-41_877-37del
NM_014916.3:c.877-41_877-37del NP_055731.2:n.877-41_877-37del
XM_011515981.1:c.871-41_871-37del XP_011514283.1:n.871-41_871-37del
XM_011515981.3:c.871-41_871-37del XP_011514283.1:n.871-41_871-37del
NM_014916.4:c.877-41_877-37del MANE Select NP_055731.2:n.877-41_877-37del