Canonical Allele Identifier: CA4355296

Gene: LMTK2

Linked Data

• dbSNP Id: rs749354416
• ExAC: 7:97816151 A / G
• gnomAD v2: 7-97816151-A-G
• gnomAD v3: 7-98186839-A-G
• gnomAD v4: 7-98186839-A-G
• MyVariant Identifiers: chr7:g.97816151A>G (hg19) ; chr7:g.98186839A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.98186839A>G , CM000669.2:g.98186839A>G	GRCh38
NC_000007.13:g.97816151A>G , CM000669.1:g.97816151A>G	GRCh37
NC_000007.12:g.97654087A>G	NCBI36
NG_013375.1:g.84955A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297293.6:c.877-38A>G MANE Select	ENSP00000297293.5:n.877-38A>G
ENST00000297293.5:c.877-38A>G	ENSP00000297293.5:n.877-38A>G
NM_014916.3:c.877-38A>G	NP_055731.2:n.877-38A>G
XM_011515981.1:c.871-38A>G	XP_011514283.1:n.871-38A>G
XM_011515981.3:c.871-38A>G	XP_011514283.1:n.871-38A>G
NM_014916.4:c.877-38A>G MANE Select	NP_055731.2:n.877-38A>G