Canonical Allele Identifier: CA1153865226
Gene: PLOD1 HGNC NCBI

Linked Data

dbSNP Id: rs1645808374

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11965348C>G , CM000663.2:g.11965348C>G GRCh38
NC_000001.10:g.12025405C>G , CM000663.1:g.12025405C>G GRCh37
NC_000001.9:g.11947992C>G NCBI36
NG_008159.1:g.35660C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000196061.5:c.1471-132C>G MANE Select ENSP00000196061.4:n.1471-132C>G
ENST00000196061.4:c.1471-132C>G ENSP00000196061.4:n.1471-132C>G
ENST00000470133.1:n.85-132C>G
ENST00000491536.5:n.99-132C>G
NM_000302.3:c.1471-132C>G NP_000293.2:n.1471-132C>G
NM_001316320.1:c.1612-132C>G NP_001303249.1:n.1612-132C>G
XM_011541594.1:c.1552-132C>G XP_011539896.1:n.1552-132C>G
XM_024447707.1:c.805-132C>G XP_024303475.1:n.805-132C>G
NM_000302.4:c.1471-132C>G MANE Select NP_000293.2:n.1471-132C>G
NM_001316320.2:c.1612-132C>G NP_001303249.1:n.1612-132C>G