Canonical Allele Identifier: CA1153865833
Gene: PLOD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11965555C= , CM000663.2:g.11965555C= GRCh38
NC_000001.10:g.12025612C= , CM000663.1:g.12025612C= GRCh37
NC_000001.9:g.11948199C= NCBI36
NG_008159.1:g.35867C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000196061.5:c.1546C= MANE Select ENSP00000196061.4:p.Leu516=
ENST00000196061.4:c.1546C= ENSP00000196061.4:p.Leu516=
ENST00000470133.1:n.160C=
ENST00000491536.5:n.174C=
NM_000302.3:c.1546C= NP_000293.2:p.Leu516=
NM_001316320.1:c.1687C= NP_001303249.1:p.Leu563=
XM_011541594.1:c.1627C= XP_011539896.1:p.Leu543=
XM_024447707.1:c.880C= XP_024303475.1:p.Leu294=
NM_000302.4:c.1546C= MANE Select NP_000293.2:p.Leu516=
NM_001316320.2:c.1687C= NP_001303249.1:p.Leu563=