Canonical Allele Identifier: CA338444765
Gene: PLOD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11965534G>C , CM000663.2:g.11965534G>C GRCh38
NC_000001.10:g.12025591G>C , CM000663.1:g.12025591G>C GRCh37
NC_000001.9:g.11948178G>C NCBI36
NG_008159.1:g.35846G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000196061.5:c.1525G>C MANE Select ENSP00000196061.4:p.Asp509His
ENST00000196061.4:c.1525G>C ENSP00000196061.4:p.Asp509His
ENST00000470133.1:n.139G>C
ENST00000491536.5:n.153G>C
NM_000302.3:c.1525G>C NP_000293.2:p.Asp509His
NM_001316320.1:c.1666G>C NP_001303249.1:p.Asp556His
XM_011541594.1:c.1606G>C XP_011539896.1:p.Asp536His
XM_024447707.1:c.859G>C XP_024303475.1:p.Asp287His
NM_000302.4:c.1525G>C MANE Select NP_000293.2:p.Asp509His
NM_001316320.2:c.1666G>C NP_001303249.1:p.Asp556His