Canonical Allele Identifier: CA1153865362
Gene: PLOD1 HGNC NCBI

Linked Data

dbSNP Id: rs1645808948
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11965402T>A , CM000663.2:g.11965402T>A GRCh38
NC_000001.10:g.12025459T>A , CM000663.1:g.12025459T>A GRCh37
NC_000001.9:g.11948046T>A NCBI36
NG_008159.1:g.35714T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000196061.5:c.1471-78T>A MANE Select ENSP00000196061.4:n.1471-78T>A
ENST00000196061.4:c.1471-78T>A ENSP00000196061.4:n.1471-78T>A
ENST00000470133.1:n.85-78T>A
ENST00000491536.5:n.99-78T>A
NM_000302.3:c.1471-78T>A NP_000293.2:n.1471-78T>A
NM_001316320.1:c.1612-78T>A NP_001303249.1:n.1612-78T>A
XM_011541594.1:c.1552-78T>A XP_011539896.1:n.1552-78T>A
XM_024447707.1:c.805-78T>A XP_024303475.1:n.805-78T>A
NM_000302.4:c.1471-78T>A MANE Select NP_000293.2:n.1471-78T>A
NM_001316320.2:c.1612-78T>A NP_001303249.1:n.1612-78T>A
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