Canonical Allele Identifier: CA1153865748
Gene: PLOD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11965525C= , CM000663.2:g.11965525C= GRCh38
NC_000001.10:g.12025582C= , CM000663.1:g.12025582C= GRCh37
NC_000001.9:g.11948169C= NCBI36
NG_008159.1:g.35837C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000196061.5:c.1516C= MANE Select ENSP00000196061.4:p.Leu506=
ENST00000196061.4:c.1516C= ENSP00000196061.4:p.Leu506=
ENST00000470133.1:n.130C=
ENST00000491536.5:n.144C=
NM_000302.3:c.1516C= NP_000293.2:p.Leu506=
NM_001316320.1:c.1657C= NP_001303249.1:p.Leu553=
XM_011541594.1:c.1597C= XP_011539896.1:p.Leu533=
XM_024447707.1:c.850C= XP_024303475.1:p.Leu284=
NM_000302.4:c.1516C= MANE Select NP_000293.2:p.Leu506=
NM_001316320.2:c.1657C= NP_001303249.1:p.Leu553=