Canonical Allele Identifier: CA1143149119
Gene: PLOD1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11965375G= , CM000663.2:g.11965375G= GRCh38
NC_000001.10:g.12025432G= , CM000663.1:g.12025432G= GRCh37
NC_000001.9:g.11948019G= NCBI36
NG_008159.1:g.35687G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000196061.5:c.1471-105G= MANE Select ENSP00000196061.4:n.1471-105G=
ENST00000196061.4:c.1471-105G= ENSP00000196061.4:n.1471-105G=
ENST00000470133.1:n.85-105G=
ENST00000491536.5:n.99-105G=
NM_000302.3:c.1471-105G= NP_000293.2:n.1471-105G=
NM_001316320.1:c.1612-105G= NP_001303249.1:n.1612-105G=
XM_011541594.1:c.1552-105G= XP_011539896.1:n.1552-105G=
XM_024447707.1:c.805-105G= XP_024303475.1:n.805-105G=
NM_000302.4:c.1471-105G= MANE Select NP_000293.2:n.1471-105G=
NM_001316320.2:c.1612-105G= NP_001303249.1:n.1612-105G=
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