Canonical Allele Identifier: CA886257507
Gene: PLOD1 HGNC NCBI

Linked Data

dbSNP Id: rs538428354
gnomAD v3: 1-11965437-A-G
gnomAD v4: 1-11965437-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11965437A>G , CM000663.2:g.11965437A>G GRCh38
NC_000001.10:g.12025494A>G , CM000663.1:g.12025494A>G GRCh37
NC_000001.9:g.11948081A>G NCBI36
NG_008159.1:g.35749A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000196061.5:c.1471-43A>G MANE Select ENSP00000196061.4:n.1471-43A>G
ENST00000196061.4:c.1471-43A>G ENSP00000196061.4:n.1471-43A>G
ENST00000470133.1:n.85-43A>G
ENST00000491536.5:n.99-43A>G
NM_000302.3:c.1471-43A>G NP_000293.2:n.1471-43A>G
NM_001316320.1:c.1612-43A>G NP_001303249.1:n.1612-43A>G
XM_011541594.1:c.1552-43A>G XP_011539896.1:n.1552-43A>G
XM_024447707.1:c.805-43A>G XP_024303475.1:n.805-43A>G
NM_000302.4:c.1471-43A>G MANE Select NP_000293.2:n.1471-43A>G
NM_001316320.2:c.1612-43A>G NP_001303249.1:n.1612-43A>G