Canonical Allele Identifier: CA338444990

Gene: PLOD1

Linked Data

• MyVariant Identifiers: chr1:g.12025611C>A (hg19) ; chr1:g.11965554C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11965554C>A , CM000663.2:g.11965554C>A	GRCh38
NC_000001.10:g.12025611C>A , CM000663.1:g.12025611C>A	GRCh37
NC_000001.9:g.11948198C>A	NCBI36
NG_008159.1:g.35866C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000196061.5:c.1545C>A MANE Select	ENSP00000196061.4:p.His515Gln
ENST00000196061.4:c.1545C>A	ENSP00000196061.4:p.His515Gln
ENST00000470133.1:n.159C>A
ENST00000491536.5:n.173C>A
NM_000302.3:c.1545C>A	NP_000293.2:p.His515Gln
NM_001316320.1:c.1686C>A	NP_001303249.1:p.His562Gln
XM_011541594.1:c.1626C>A	XP_011539896.1:p.His542Gln
XM_024447707.1:c.879C>A	XP_024303475.1:p.His293Gln
NM_000302.4:c.1545C>A MANE Select	NP_000293.2:p.His515Gln
NM_001316320.2:c.1686C>A	NP_001303249.1:p.His562Gln