Canonical Allele Identifier: CA598120

Gene: PLOD1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11957833C>G , CM000663.2:g.11957833C>G	GRCh38
NC_000001.10:g.12017890C>G , CM000663.1:g.12017890C>G	GRCh37
NC_000001.9:g.11940477C>G	NCBI36
NG_008159.1:g.28145C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000196061.5:c.742-9C>G MANE Select	ENSP00000196061.4:n.742-9C>G
ENST00000196061.4:c.742-9C>G	ENSP00000196061.4:n.742-9C>G
ENST00000429000.6:c.748-9C>G	ENSP00000405372.1:n.748-9C>G
ENST00000465920.1:n.692-9C>G
ENST00000485046.5:n.785-9C>G
NM_000302.3:c.742-9C>G	NP_000293.2:n.742-9C>G
NM_001316320.1:c.883-9C>G	NP_001303249.1:n.883-9C>G
XM_011541594.1:c.823-9C>G	XP_011539896.1:n.823-9C>G
XM_024447707.1:c.76-9C>G	XP_024303475.1:n.76-9C>G
NM_000302.4:c.742-9C>G MANE Select	NP_000293.2:n.742-9C>G
NM_001316320.2:c.883-9C>G	NP_001303249.1:n.883-9C>G