Canonical Allele Identifier: CA1153865463
Gene: PLOD1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11965431C= , CM000663.2:g.11965431C= GRCh38
NC_000001.10:g.12025488C= , CM000663.1:g.12025488C= GRCh37
NC_000001.9:g.11948075C= NCBI36
NG_008159.1:g.35743C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000196061.5:c.1471-49C= MANE Select ENSP00000196061.4:n.1471-49C=
ENST00000196061.4:c.1471-49C= ENSP00000196061.4:n.1471-49C=
ENST00000470133.1:n.85-49C=
ENST00000491536.5:n.99-49C=
NM_000302.3:c.1471-49C= NP_000293.2:n.1471-49C=
NM_001316320.1:c.1612-49C= NP_001303249.1:n.1612-49C=
XM_011541594.1:c.1552-49C= XP_011539896.1:n.1552-49C=
XM_024447707.1:c.805-49C= XP_024303475.1:n.805-49C=
NM_000302.4:c.1471-49C= MANE Select NP_000293.2:n.1471-49C=
NM_001316320.2:c.1612-49C= NP_001303249.1:n.1612-49C=
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