Canonical Allele Identifier: CA406681065
Gene: LMTK3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48499307G>C , CM000681.2:g.48499307G>C GRCh38
NC_000019.9:g.49002564G>C , CM000681.1:g.49002564G>C GRCh37
NC_000019.8:g.53694376G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001388485.1:c.1762C>G MANE Select NP_001375414.1:p.Leu588Val
ENST00000600059.6:c.1762C>G MANE Select ENSP00000472020.1:p.Leu588Val
NM_001080434.1:c.1849C>G NP_001073903.1:p.Leu617Val
NM_001080434.2:c.1762C>G NP_001073903.2:p.Leu588Val
ENST00000270238.3:c.1849C>G ENSP00000270238.3:p.Leu617Val
ENST00000600059.5:c.1762C>G ENSP00000472020.1:p.Leu588Val
ENST00000650440.1:c.1840C>G ENSP00000497480.1:p.Leu614Val
ENST00000672160.1:c.1027C>G ENSP00000500093.1:p.Leu343Val
ENST00000673139.1:c.1762C>G ENSP00000500153.1:p.Leu588Val
XM_011526411.1:c.1840C>G XP_011524713.1:p.Leu614Val
XM_011526411.2:c.1840C>G XP_011524713.1:p.Leu614Val
XM_011526412.1:c.1807C>G XP_011524714.1:p.Leu603Val
XM_011526412.2:c.1807C>G XP_011524714.1:p.Leu603Val