Canonical Allele Identifier: CA338444379
Gene: PLOD1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.12025545C>A (hg19) chr1:g.11965488C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11965488C>A , CM000663.2:g.11965488C>A GRCh38
NC_000001.10:g.12025545C>A , CM000663.1:g.12025545C>A GRCh37
NC_000001.9:g.11948132C>A NCBI36
NG_008159.1:g.35800C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000196061.5:c.1479C>A MANE Select ENSP00000196061.4:p.Phe493Leu
ENST00000196061.4:c.1479C>A ENSP00000196061.4:p.Phe493Leu
ENST00000470133.1:n.93C>A
ENST00000491536.5:n.107C>A
NM_000302.3:c.1479C>A NP_000293.2:p.Phe493Leu
NM_001316320.1:c.1620C>A NP_001303249.1:p.Phe540Leu
XM_011541594.1:c.1560C>A XP_011539896.1:p.Phe520Leu
XM_024447707.1:c.813C>A XP_024303475.1:p.Phe271Leu
NM_000302.4:c.1479C>A MANE Select NP_000293.2:p.Phe493Leu
NM_001316320.2:c.1620C>A NP_001303249.1:p.Phe540Leu
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