Canonical Allele Identifier: CA1153865445
Gene: PLOD1 HGNC NCBI

Linked Data

dbSNP Id: rs1379204584
gnomAD v4: 1-11965424-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11965424G>A , CM000663.2:g.11965424G>A GRCh38
NC_000001.10:g.12025481G>A , CM000663.1:g.12025481G>A GRCh37
NC_000001.9:g.11948068G>A NCBI36
NG_008159.1:g.35736G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000196061.5:c.1471-56G>A MANE Select ENSP00000196061.4:n.1471-56G>A
ENST00000196061.4:c.1471-56G>A ENSP00000196061.4:n.1471-56G>A
ENST00000470133.1:n.85-56G>A
ENST00000491536.5:n.99-56G>A
NM_000302.3:c.1471-56G>A NP_000293.2:n.1471-56G>A
NM_001316320.1:c.1612-56G>A NP_001303249.1:n.1612-56G>A
XM_011541594.1:c.1552-56G>A XP_011539896.1:n.1552-56G>A
XM_024447707.1:c.805-56G>A XP_024303475.1:n.805-56G>A
NM_000302.4:c.1471-56G>A MANE Select NP_000293.2:n.1471-56G>A
NM_001316320.2:c.1612-56G>A NP_001303249.1:n.1612-56G>A