Canonical Allele Identifier: CA1153865727

Gene: PLOD1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11965512C= , CM000663.2:g.11965512C=	GRCh38
NC_000001.10:g.12025569C= , CM000663.1:g.12025569C=	GRCh37
NC_000001.9:g.11948156C=	NCBI36
NG_008159.1:g.35824C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000196061.5:c.1503C= MANE Select	ENSP00000196061.4:p.Thr501=
ENST00000196061.4:c.1503C=	ENSP00000196061.4:p.Thr501=
ENST00000470133.1:n.117C=
ENST00000491536.5:n.131C=
NM_000302.3:c.1503C=	NP_000293.2:p.Thr501=
NM_001316320.1:c.1644C=	NP_001303249.1:p.Thr548=
XM_011541594.1:c.1584C=	XP_011539896.1:p.Thr528=
XM_024447707.1:c.837C=	XP_024303475.1:p.Thr279=
NM_000302.4:c.1503C= MANE Select	NP_000293.2:p.Thr501=
NM_001316320.2:c.1644C=	NP_001303249.1:p.Thr548=