Canonical Allele Identifier: CA338444828
Gene: PLOD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11965539C>A , CM000663.2:g.11965539C>A GRCh38
NC_000001.10:g.12025596C>A , CM000663.1:g.12025596C>A GRCh37
NC_000001.9:g.11948183C>A NCBI36
NG_008159.1:g.35851C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000196061.5:c.1530C>A MANE Select ENSP00000196061.4:p.Ser510Arg
ENST00000196061.4:c.1530C>A ENSP00000196061.4:p.Ser510Arg
ENST00000470133.1:n.144C>A
ENST00000491536.5:n.158C>A
NM_000302.3:c.1530C>A NP_000293.2:p.Ser510Arg
NM_001316320.1:c.1671C>A NP_001303249.1:p.Ser557Arg
XM_011541594.1:c.1611C>A XP_011539896.1:p.Ser537Arg
XM_024447707.1:c.864C>A XP_024303475.1:p.Ser288Arg
NM_000302.4:c.1530C>A MANE Select NP_000293.2:p.Ser510Arg
NM_001316320.2:c.1671C>A NP_001303249.1:p.Ser557Arg