Canonical Allele Identifier: CA416107660
Gene: PLOD1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.12025587C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11965530C>A , CM000663.2:g.11965530C>A GRCh38
NC_000001.10:g.12025587C>A , CM000663.1:g.12025587C>A GRCh37
NC_000001.9:g.11948174C>A NCBI36
NG_008159.1:g.35842C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000196061.5:c.1521C>A MANE Select ENSP00000196061.4:p.Ser507=
ENST00000196061.4:c.1521C>A ENSP00000196061.4:p.Ser507=
ENST00000470133.1:n.135C>A
ENST00000491536.5:n.149C>A
NM_000302.3:c.1521C>A NP_000293.2:p.Ser507=
NM_001316320.1:c.1662C>A NP_001303249.1:p.Ser554=
XM_011541594.1:c.1602C>A XP_011539896.1:p.Ser534=
XM_024447707.1:c.855C>A XP_024303475.1:p.Ser285=
NM_000302.4:c.1521C>A MANE Select NP_000293.2:p.Ser507=
NM_001316320.2:c.1662C>A NP_001303249.1:p.Ser554=
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Search 100 bp 3'