Canonical Allele Identifier: CA18013955

Gene: PLOD1

Linked Data

• dbSNP Id: rs916806668
• gnomAD v4: 1-11965409-G-A
• MyVariant Identifiers: chr1:g.12025466G>A (hg19) ; chr1:g.11965409G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11965409G>A , CM000663.2:g.11965409G>A	GRCh38
NC_000001.10:g.12025466G>A , CM000663.1:g.12025466G>A	GRCh37
NC_000001.9:g.11948053G>A	NCBI36
NG_008159.1:g.35721G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000196061.5:c.1471-71G>A MANE Select	ENSP00000196061.4:n.1471-71G>A
ENST00000196061.4:c.1471-71G>A	ENSP00000196061.4:n.1471-71G>A
ENST00000470133.1:n.85-71G>A
ENST00000491536.5:n.99-71G>A
NM_000302.3:c.1471-71G>A	NP_000293.2:n.1471-71G>A
NM_001316320.1:c.1612-71G>A	NP_001303249.1:n.1612-71G>A
XM_011541594.1:c.1552-71G>A	XP_011539896.1:n.1552-71G>A
XM_024447707.1:c.805-71G>A	XP_024303475.1:n.805-71G>A
NM_000302.4:c.1471-71G>A MANE Select	NP_000293.2:n.1471-71G>A
NM_001316320.2:c.1612-71G>A	NP_001303249.1:n.1612-71G>A