Canonical Allele Identifier: CA338444403
Gene: PLOD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11965492T>A , CM000663.2:g.11965492T>A GRCh38
NC_000001.10:g.12025549T>A , CM000663.1:g.12025549T>A GRCh37
NC_000001.9:g.11948136T>A NCBI36
NG_008159.1:g.35804T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000196061.5:c.1483T>A MANE Select ENSP00000196061.4:p.Phe495Ile
ENST00000196061.4:c.1483T>A ENSP00000196061.4:p.Phe495Ile
ENST00000470133.1:n.97T>A
ENST00000491536.5:n.111T>A
NM_000302.3:c.1483T>A NP_000293.2:p.Phe495Ile
NM_001316320.1:c.1624T>A NP_001303249.1:p.Phe542Ile
XM_011541594.1:c.1564T>A XP_011539896.1:p.Phe522Ile
XM_024447707.1:c.817T>A XP_024303475.1:p.Phe273Ile
NM_000302.4:c.1483T>A MANE Select NP_000293.2:p.Phe495Ile
NM_001316320.2:c.1624T>A NP_001303249.1:p.Phe542Ile