Canonical Allele Identifier: CA338445497

Gene: PLOD1

Linked Data

• MyVariant Identifiers: chr1:g.12025652T>A (hg19) ; chr1:g.11965595T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11965595T>A , CM000663.2:g.11965595T>A	GRCh38
NC_000001.10:g.12025652T>A , CM000663.1:g.12025652T>A	GRCh37
NC_000001.9:g.11948239T>A	NCBI36
NG_008159.1:g.35907T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000196061.5:c.1584+2T>A MANE Select	ENSP00000196061.4:n.1584+2T>A
ENST00000196061.4:c.1584+2T>A	ENSP00000196061.4:n.1584+2T>A
ENST00000470133.1:n.198+2T>A
ENST00000491536.5:n.212+2T>A
NM_000302.3:c.1584+2T>A	NP_000293.2:n.1584+2T>A
NM_001316320.1:c.1725+2T>A	NP_001303249.1:n.1725+2T>A
XM_011541594.1:c.1665+2T>A	XP_011539896.1:n.1665+2T>A
XM_024447707.1:c.918+2T>A	XP_024303475.1:n.918+2T>A
NM_000302.4:c.1584+2T>A MANE Select	NP_000293.2:n.1584+2T>A
NM_001316320.2:c.1725+2T>A	NP_001303249.1:n.1725+2T>A