Canonical Allele Identifier: CA2592850037
Gene: PLOD1 HGNC NCBI

Linked Data

gnomAD v3: 1-11965403-C-G
gnomAD v4: 1-11965403-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11965403C>G , CM000663.2:g.11965403C>G GRCh38
NC_000001.10:g.12025460C>G , CM000663.1:g.12025460C>G GRCh37
NC_000001.9:g.11948047C>G NCBI36
NG_008159.1:g.35715C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000196061.5:c.1471-77C>G MANE Select ENSP00000196061.4:n.1471-77C>G
ENST00000196061.4:c.1471-77C>G ENSP00000196061.4:n.1471-77C>G
ENST00000470133.1:n.85-77C>G
ENST00000491536.5:n.99-77C>G
NM_000302.3:c.1471-77C>G NP_000293.2:n.1471-77C>G
NM_001316320.1:c.1612-77C>G NP_001303249.1:n.1612-77C>G
XM_011541594.1:c.1552-77C>G XP_011539896.1:n.1552-77C>G
XM_024447707.1:c.805-77C>G XP_024303475.1:n.805-77C>G
NM_000302.4:c.1471-77C>G MANE Select NP_000293.2:n.1471-77C>G
NM_001316320.2:c.1612-77C>G NP_001303249.1:n.1612-77C>G