Canonical Allele Identifier: CA338444890
Gene: PLOD1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.12025599C>A (hg19) chr1:g.11965542C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11965542C>A , CM000663.2:g.11965542C>A GRCh38
NC_000001.10:g.12025599C>A , CM000663.1:g.12025599C>A GRCh37
NC_000001.9:g.11948186C>A NCBI36
NG_008159.1:g.35854C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000196061.5:c.1533C>A MANE Select ENSP00000196061.4:p.Tyr511Ter
ENST00000196061.4:c.1533C>A ENSP00000196061.4:p.Tyr511Ter
ENST00000470133.1:n.147C>A
ENST00000491536.5:n.161C>A
NM_000302.3:c.1533C>A NP_000293.2:p.Tyr511Ter
NM_001316320.1:c.1674C>A NP_001303249.1:p.Tyr558Ter
XM_011541594.1:c.1614C>A XP_011539896.1:p.Tyr538Ter
XM_024447707.1:c.867C>A XP_024303475.1:p.Tyr289Ter
NM_000302.4:c.1533C>A MANE Select NP_000293.2:p.Tyr511Ter
NM_001316320.2:c.1674C>A NP_001303249.1:p.Tyr558Ter
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