Canonical Allele Identifier: CA1153865922
Gene: PLOD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11965567C= , CM000663.2:g.11965567C= GRCh38
NC_000001.10:g.12025624C= , CM000663.1:g.12025624C= GRCh37
NC_000001.9:g.11948211C= NCBI36
NG_008159.1:g.35879C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000196061.5:c.1558C= MANE Select ENSP00000196061.4:p.Leu520=
ENST00000196061.4:c.1558C= ENSP00000196061.4:p.Leu520=
ENST00000470133.1:n.172C=
ENST00000491536.5:n.186C=
NM_000302.3:c.1558C= NP_000293.2:p.Leu520=
NM_001316320.1:c.1699C= NP_001303249.1:p.Leu567=
XM_011541594.1:c.1639C= XP_011539896.1:p.Leu547=
XM_024447707.1:c.892C= XP_024303475.1:p.Leu298=
NM_000302.4:c.1558C= MANE Select NP_000293.2:p.Leu520=
NM_001316320.2:c.1699C= NP_001303249.1:p.Leu567=