Canonical Allele Identifier: CA598036
Gene: PLOD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11956900T>G , CM000663.2:g.11956900T>G GRCh38
NC_000001.10:g.12016957T>G , CM000663.1:g.12016957T>G GRCh37
NC_000001.9:g.11939544T>G NCBI36
NG_008159.1:g.27212T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000196061.5:c.644-17T>G MANE Select ENSP00000196061.4:n.644-17T>G
ENST00000196061.4:c.644-17T>G ENSP00000196061.4:n.644-17T>G
ENST00000429000.6:c.644-190T>G ENSP00000405372.1:n.644-190T>G
ENST00000465920.1:n.594-17T>G
ENST00000485046.5:n.687-17T>G
NM_000302.3:c.644-17T>G NP_000293.2:n.644-17T>G
NM_001316320.1:c.785-17T>G NP_001303249.1:n.785-17T>G
XM_011541594.1:c.725-17T>G XP_011539896.1:n.725-17T>G
XM_024447707.1:c.-23-17T>G XP_024303475.1:n.-23-17T>G
NM_000302.4:c.644-17T>G MANE Select NP_000293.2:n.644-17T>G
NM_001316320.2:c.785-17T>G NP_001303249.1:n.785-17T>G