Canonical Allele Identifier: CA1728472135
Gene: LMTK2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98186967A= , CM000669.2:g.98186967A= GRCh38
NC_000007.13:g.97816279A= , CM000669.1:g.97816279A= GRCh37
NC_000007.12:g.97654215A= NCBI36
NG_013375.1:g.85083A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.967A= MANE Select ENSP00000297293.5:p.Thr323=
ENST00000297293.5:c.967A= ENSP00000297293.5:p.Thr323=
NM_014916.3:c.967A= NP_055731.2:p.Thr323=
XM_011515981.1:c.961A= XP_011514283.1:p.Thr321=
XM_011515981.3:c.961A= XP_011514283.1:p.Thr321=
NM_014916.4:c.967A= MANE Select NP_055731.2:p.Thr323=
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