Canonical Allele Identifier: CA1140429502
Gene: PLOD1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11965453C= , CM000663.2:g.11965453C= GRCh38
NC_000001.10:g.12025510C= , CM000663.1:g.12025510C= GRCh37
NC_000001.9:g.11948097C= NCBI36
NG_008159.1:g.35765C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000196061.5:c.1471-27C= MANE Select ENSP00000196061.4:n.1471-27C=
ENST00000196061.4:c.1471-27C= ENSP00000196061.4:n.1471-27C=
ENST00000470133.1:n.85-27C=
ENST00000491536.5:n.99-27C=
NM_000302.3:c.1471-27C= NP_000293.2:n.1471-27C=
NM_001316320.1:c.1612-27C= NP_001303249.1:n.1612-27C=
XM_011541594.1:c.1552-27C= XP_011539896.1:n.1552-27C=
XM_024447707.1:c.805-27C= XP_024303475.1:n.805-27C=
NM_000302.4:c.1471-27C= MANE Select NP_000293.2:n.1471-27C=
NM_001316320.2:c.1612-27C= NP_001303249.1:n.1612-27C=
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