Canonical Allele Identifier: CA368270002
Gene: LMTK2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.97816263T>G (hg19) chr7:g.98186951T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98186951T>G , CM000669.2:g.98186951T>G GRCh38
NC_000007.13:g.97816263T>G , CM000669.1:g.97816263T>G GRCh37
NC_000007.12:g.97654199T>G NCBI36
NG_013375.1:g.85067T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.951T>G MANE Select ENSP00000297293.5:p.Phe317Leu
ENST00000297293.5:c.951T>G ENSP00000297293.5:p.Phe317Leu
NM_014916.3:c.951T>G NP_055731.2:p.Phe317Leu
XM_011515981.1:c.945T>G XP_011514283.1:p.Phe315Leu
XM_011515981.3:c.945T>G XP_011514283.1:p.Phe315Leu
NM_014916.4:c.951T>G MANE Select NP_055731.2:p.Phe317Leu
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