Canonical Allele Identifier: CA1104852682

Gene: LMTK2

Linked Data

• dbSNP Id: rs1797449557
• gnomAD v3: 7-98187236-AG-A
• gnomAD v4: 7-98187236-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.98187237del , CM000669.2:g.98187237del	GRCh38
NC_000007.13:g.97816549del , CM000669.1:g.97816549del	GRCh37
NC_000007.12:g.97654485del	NCBI36
NG_013375.1:g.85353del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297293.6:c.998+239del MANE Select	ENSP00000297293.5:n.998+239del
ENST00000297293.5:c.998+239del	ENSP00000297293.5:n.998+239del
NM_014916.3:c.998+239del	NP_055731.2:n.998+239del
XM_011515981.1:c.992+239del	XP_011514283.1:n.992+239del
XM_011515981.3:c.992+239del	XP_011514283.1:n.992+239del
NM_014916.4:c.998+239del MANE Select	NP_055731.2:n.998+239del