Canonical Allele Identifier: CA338445369

Gene: PLOD1

Linked Data

• MyVariant Identifiers: chr1:g.12025642A>C (hg19) ; chr1:g.11965585A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11965585A>C , CM000663.2:g.11965585A>C	GRCh38
NC_000001.10:g.12025642A>C , CM000663.1:g.12025642A>C	GRCh37
NC_000001.9:g.11948229A>C	NCBI36
NG_008159.1:g.35897A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000196061.5:c.1576A>C MANE Select	ENSP00000196061.4:p.Asn526His
ENST00000196061.4:c.1576A>C	ENSP00000196061.4:p.Asn526His
ENST00000470133.1:n.190A>C
ENST00000491536.5:n.204A>C
NM_000302.3:c.1576A>C	NP_000293.2:p.Asn526His
NM_001316320.1:c.1717A>C	NP_001303249.1:p.Asn573His
XM_011541594.1:c.1657A>C	XP_011539896.1:p.Asn553His
XM_024447707.1:c.910A>C	XP_024303475.1:p.Asn304His
NM_000302.4:c.1576A>C MANE Select	NP_000293.2:p.Asn526His
NM_001316320.2:c.1717A>C	NP_001303249.1:p.Asn573His