Canonical Allele Identifier: CA1153865648
Gene: PLOD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11965491G= , CM000663.2:g.11965491G= GRCh38
NC_000001.10:g.12025548G= , CM000663.1:g.12025548G= GRCh37
NC_000001.9:g.11948135G= NCBI36
NG_008159.1:g.35803G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000196061.5:c.1482G= MANE Select ENSP00000196061.4:p.Met494=
ENST00000196061.4:c.1482G= ENSP00000196061.4:p.Met494=
ENST00000470133.1:n.96G=
ENST00000491536.5:n.110G=
NM_000302.3:c.1482G= NP_000293.2:p.Met494=
NM_001316320.1:c.1623G= NP_001303249.1:p.Met541=
XM_011541594.1:c.1563G= XP_011539896.1:p.Met521=
XM_024447707.1:c.816G= XP_024303475.1:p.Met272=
NM_000302.4:c.1482G= MANE Select NP_000293.2:p.Met494=
NM_001316320.2:c.1623G= NP_001303249.1:p.Met541=