Canonical Allele Identifier: CA576377441

Gene: LMTK2

Linked Data

• dbSNP Id: rs1562918694
• gnomAD v2: 7-97816620-G-A
• gnomAD v3: 7-98187308-G-A
• gnomAD v4: 7-98187308-G-A
• MyVariant Identifiers: chr7:g.97816620G>A (hg19) ; chr7:g.98187308G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.98187308G>A , CM000669.2:g.98187308G>A	GRCh38
NC_000007.13:g.97816620G>A , CM000669.1:g.97816620G>A	GRCh37
NC_000007.12:g.97654556G>A	NCBI36
NG_013375.1:g.85424G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297293.6:c.998+310G>A MANE Select	ENSP00000297293.5:n.998+310G>A
ENST00000297293.5:c.998+310G>A	ENSP00000297293.5:n.998+310G>A
NM_014916.3:c.998+310G>A	NP_055731.2:n.998+310G>A
XM_011515981.1:c.992+310G>A	XP_011514283.1:n.992+310G>A
XM_011515981.3:c.992+310G>A	XP_011514283.1:n.992+310G>A
NM_014916.4:c.998+310G>A MANE Select	NP_055731.2:n.998+310G>A