Canonical Allele Identifier: CA338444552

Gene: PLOD1

Linked Data

• MyVariant Identifiers: chr1:g.12025567A>T (hg19) ; chr1:g.11965510A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11965510A>T , CM000663.2:g.11965510A>T	GRCh38
NC_000001.10:g.12025567A>T , CM000663.1:g.12025567A>T	GRCh37
NC_000001.9:g.11948154A>T	NCBI36
NG_008159.1:g.35822A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000196061.5:c.1501A>T MANE Select	ENSP00000196061.4:p.Thr501Ser
ENST00000196061.4:c.1501A>T	ENSP00000196061.4:p.Thr501Ser
ENST00000470133.1:n.115A>T
ENST00000491536.5:n.129A>T
NM_000302.3:c.1501A>T	NP_000293.2:p.Thr501Ser
NM_001316320.1:c.1642A>T	NP_001303249.1:p.Thr548Ser
XM_011541594.1:c.1582A>T	XP_011539896.1:p.Thr528Ser
XM_024447707.1:c.835A>T	XP_024303475.1:p.Thr279Ser
NM_000302.4:c.1501A>T MANE Select	NP_000293.2:p.Thr501Ser
NM_001316320.2:c.1642A>T	NP_001303249.1:p.Thr548Ser