Canonical Allele Identifier: CA368269950
Gene: LMTK2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.97816251A>C (hg19) chr7:g.98186939A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98186939A>C , CM000669.2:g.98186939A>C GRCh38
NC_000007.13:g.97816251A>C , CM000669.1:g.97816251A>C GRCh37
NC_000007.12:g.97654187A>C NCBI36
NG_013375.1:g.85055A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000297293.6:c.939A>C MANE Select ENSP00000297293.5:p.Leu313Phe
ENST00000297293.5:c.939A>C ENSP00000297293.5:p.Leu313Phe
NM_014916.3:c.939A>C NP_055731.2:p.Leu313Phe
XM_011515981.1:c.933A>C XP_011514283.1:p.Leu311Phe
XM_011515981.3:c.933A>C XP_011514283.1:p.Leu311Phe
NM_014916.4:c.939A>C MANE Select NP_055731.2:p.Leu313Phe
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