Canonical Allele Identifier: CA2339932565

Gene: LMTK3

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48510834T>A , CM000681.2:g.48510834T>A	GRCh38
NC_000019.9:g.49014091T>A , CM000681.1:g.49014091T>A	GRCh37
NC_000019.8:g.53705903T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000600059.6:c.77-242A>T MANE Select	ENSP00000472020.1:n.77-242A>T
ENST00000647709.2:c.77-242A>T	ENSP00000496937.2:n.77-242A>T
ENST00000650440.1:c.155-242A>T	ENSP00000497480.1:n.155-242A>T
ENST00000673139.1:c.77-242A>T	ENSP00000500153.1:n.77-242A>T
ENST00000270238.3:c.164-242A>T	ENSP00000270238.3:n.164-242A>T
ENST00000600059.5:c.77-242A>T	ENSP00000472020.1:n.77-242A>T
NM_001080434.1:c.164-242A>T	NP_001073903.1:n.164-242A>T
XM_011526411.1:c.155-242A>T	XP_011524713.1:n.155-242A>T
XM_011526412.1:c.122-242A>T	XP_011524714.1:n.122-242A>T
XM_011526411.2:c.155-242A>T	XP_011524713.1:n.155-242A>T
XM_011526412.2:c.122-242A>T	XP_011524714.1:n.122-242A>T
NM_001080434.2:c.77-242A>T	NP_001073903.2:n.77-242A>T
NM_001388485.1:c.77-242A>T MANE Select	NP_001375414.1:n.77-242A>T