Canonical Allele Identifier: CA338444498
Gene: PLOD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11965505G>T , CM000663.2:g.11965505G>T GRCh38
NC_000001.10:g.12025562G>T , CM000663.1:g.12025562G>T GRCh37
NC_000001.9:g.11948149G>T NCBI36
NG_008159.1:g.35817G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000196061.5:c.1496G>T MANE Select ENSP00000196061.4:p.Arg499Leu
ENST00000196061.4:c.1496G>T ENSP00000196061.4:p.Arg499Leu
ENST00000470133.1:n.110G>T
ENST00000491536.5:n.124G>T
NM_000302.3:c.1496G>T NP_000293.2:p.Arg499Leu
NM_001316320.1:c.1637G>T NP_001303249.1:p.Arg546Leu
XM_011541594.1:c.1577G>T XP_011539896.1:p.Arg526Leu
XM_024447707.1:c.830G>T XP_024303475.1:p.Arg277Leu
NM_000302.4:c.1496G>T MANE Select NP_000293.2:p.Arg499Leu
NM_001316320.2:c.1637G>T NP_001303249.1:p.Arg546Leu