Canonical Allele Identifier: CA456635203
Gene: LMTK2 HGNC NCBI

Linked Data

COSMIC: COSM4993034 COSM4993035
MyVariant Identifiers: chr7:g.97816254A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98186942A>G , CM000669.2:g.98186942A>G GRCh38
NC_000007.13:g.97816254A>G , CM000669.1:g.97816254A>G GRCh37
NC_000007.12:g.97654190A>G NCBI36
NG_013375.1:g.85058A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.942A>G MANE Select ENSP00000297293.5:p.Val314=
ENST00000297293.5:c.942A>G ENSP00000297293.5:p.Val314=
NM_014916.3:c.942A>G NP_055731.2:p.Val314=
XM_011515981.1:c.936A>G XP_011514283.1:p.Val312=
XM_011515981.3:c.936A>G XP_011514283.1:p.Val312=
NM_014916.4:c.942A>G MANE Select NP_055731.2:p.Val314=
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