Canonical Allele Identifier: CA338444656
Gene: PLOD1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.12025580T>A (hg19) chr1:g.11965523T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11965523T>A , CM000663.2:g.11965523T>A GRCh38
NC_000001.10:g.12025580T>A , CM000663.1:g.12025580T>A GRCh37
NC_000001.9:g.11948167T>A NCBI36
NG_008159.1:g.35835T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000196061.5:c.1514T>A MANE Select ENSP00000196061.4:p.Leu505Gln
ENST00000196061.4:c.1514T>A ENSP00000196061.4:p.Leu505Gln
ENST00000470133.1:n.128T>A
ENST00000491536.5:n.142T>A
NM_000302.3:c.1514T>A NP_000293.2:p.Leu505Gln
NM_001316320.1:c.1655T>A NP_001303249.1:p.Leu552Gln
XM_011541594.1:c.1595T>A XP_011539896.1:p.Leu532Gln
XM_024447707.1:c.848T>A XP_024303475.1:p.Leu283Gln
NM_000302.4:c.1514T>A MANE Select NP_000293.2:p.Leu505Gln
NM_001316320.2:c.1655T>A NP_001303249.1:p.Leu552Gln
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