Canonical Allele Identifier: CA1153865782
Gene: PLOD1 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000196061.5:c.1530C= MANE Select ENSP00000196061.4:p.Ser510=
ENST00000196061.4:c.1530C= ENSP00000196061.4:p.Ser510=
ENST00000470133.1:n.144C=
ENST00000491536.5:n.158C=
NM_000302.3:c.1530C= NP_000293.2:p.Ser510=
NM_001316320.1:c.1671C= NP_001303249.1:p.Ser557=
XM_011541594.1:c.1611C= XP_011539896.1:p.Ser537=
XM_024447707.1:c.864C= XP_024303475.1:p.Ser288=
NM_000302.4:c.1530C= MANE Select NP_000293.2:p.Ser510=
NM_001316320.2:c.1671C= NP_001303249.1:p.Ser557=