Canonical Allele Identifier: CA844372482

Gene: LMTK2

Linked Data

• dbSNP Id: rs1338429463
• gnomAD v3: 7-98187073-TAAAGG-T
• gnomAD v4: 7-98187073-TAAAGG-T
• MyVariant Identifiers: chr7:g.97816386_97816390del (hg19) ; chr7:g.98187074_98187078del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.98187078_98187082del , CM000669.2:g.98187078_98187082del	GRCh38
NC_000007.13:g.97816390_97816394del , CM000669.1:g.97816390_97816394del	GRCh37
NC_000007.12:g.97654326_97654330del	NCBI36
NG_013375.1:g.85194_85198del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297293.6:c.998+80_998+84del MANE Select	ENSP00000297293.5:n.998+80_998+84del
ENST00000297293.5:c.998+80_998+84del	ENSP00000297293.5:n.998+80_998+84del
NM_014916.3:c.998+80_998+84del	NP_055731.2:n.998+80_998+84del
XM_011515981.1:c.992+80_992+84del	XP_011514283.1:n.992+80_992+84del
XM_011515981.3:c.992+80_992+84del	XP_011514283.1:n.992+80_992+84del
NM_014916.4:c.998+80_998+84del MANE Select	NP_055731.2:n.998+80_998+84del