Canonical Allele Identifier: CA1728472101
Gene: LMTK2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98186849A= , CM000669.2:g.98186849A= GRCh38
NC_000007.13:g.97816161A= , CM000669.1:g.97816161A= GRCh37
NC_000007.12:g.97654097A= NCBI36
NG_013375.1:g.84965A=

Transcript Alleles

HGVS Amino-acid change
ENST00000297293.6:c.877-28A= MANE Select ENSP00000297293.5:n.877-28A=
ENST00000297293.5:c.877-28A= ENSP00000297293.5:n.877-28A=
NM_014916.3:c.877-28A= NP_055731.2:n.877-28A=
XM_011515981.1:c.871-28A= XP_011514283.1:n.871-28A=
XM_011515981.3:c.871-28A= XP_011514283.1:n.871-28A=
NM_014916.4:c.877-28A= MANE Select NP_055731.2:n.877-28A=
Search 100 bp 5'
Search 100 bp 3'