Canonical Allele Identifier: CA338444363
Gene: PLOD1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.12025544T>C (hg19) chr1:g.11965487T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11965487T>C , CM000663.2:g.11965487T>C GRCh38
NC_000001.10:g.12025544T>C , CM000663.1:g.12025544T>C GRCh37
NC_000001.9:g.11948131T>C NCBI36
NG_008159.1:g.35799T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000196061.5:c.1478T>C MANE Select ENSP00000196061.4:p.Phe493Ser
ENST00000196061.4:c.1478T>C ENSP00000196061.4:p.Phe493Ser
ENST00000470133.1:n.92T>C
ENST00000491536.5:n.106T>C
NM_000302.3:c.1478T>C NP_000293.2:p.Phe493Ser
NM_001316320.1:c.1619T>C NP_001303249.1:p.Phe540Ser
XM_011541594.1:c.1559T>C XP_011539896.1:p.Phe520Ser
XM_024447707.1:c.812T>C XP_024303475.1:p.Phe271Ser
NM_000302.4:c.1478T>C MANE Select NP_000293.2:p.Phe493Ser
NM_001316320.2:c.1619T>C NP_001303249.1:p.Phe540Ser
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