Canonical Allele Identifier: CA163034650
Gene: LMTK2 HGNC NCBI

Linked Data

dbSNP Id: rs746711285
gnomAD v2: 7-97816620-G-GA
gnomAD v3: 7-98187308-G-GA
gnomAD v4: 7-98187308-G-GA
MyVariant Identifiers: chr7:g.97816620_97816621insA (hg19) chr7:g.98187308_98187309insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98187311dup , CM000669.2:g.98187311dup GRCh38
NC_000007.13:g.97816623dup , CM000669.1:g.97816623dup GRCh37
NC_000007.12:g.97654559dup NCBI36
NG_013375.1:g.85427dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.998+313dup MANE Select ENSP00000297293.5:n.998+313dup
ENST00000297293.5:c.998+313dup ENSP00000297293.5:n.998+313dup
NM_014916.3:c.998+313dup NP_055731.2:n.998+313dup
XM_011515981.1:c.992+313dup XP_011514283.1:n.992+313dup
XM_011515981.3:c.992+313dup XP_011514283.1:n.992+313dup
NM_014916.4:c.998+313dup MANE Select NP_055731.2:n.998+313dup
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