Canonical Allele Identifier: CA1153865699

Gene: PLOD1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11965506G= , CM000663.2:g.11965506G=	GRCh38
NC_000001.10:g.12025563G= , CM000663.1:g.12025563G=	GRCh37
NC_000001.9:g.11948150G=	NCBI36
NG_008159.1:g.35818G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000196061.5:c.1497G= MANE Select	ENSP00000196061.4:p.Arg499=
ENST00000196061.4:c.1497G=	ENSP00000196061.4:p.Arg499=
ENST00000470133.1:n.111G=
ENST00000491536.5:n.125G=
NM_000302.3:c.1497G=	NP_000293.2:p.Arg499=
NM_001316320.1:c.1638G=	NP_001303249.1:p.Arg546=
XM_011541594.1:c.1578G=	XP_011539896.1:p.Arg526=
XM_024447707.1:c.831G=	XP_024303475.1:p.Arg277=
NM_000302.4:c.1497G= MANE Select	NP_000293.2:p.Arg499=
NM_001316320.2:c.1638G=	NP_001303249.1:p.Arg546=