Canonical Allele Identifier: CA1153865618
Gene: PLOD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11965486T= , CM000663.2:g.11965486T= GRCh38
NC_000001.10:g.12025543T= , CM000663.1:g.12025543T= GRCh37
NC_000001.9:g.11948130T= NCBI36
NG_008159.1:g.35798T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000196061.5:c.1477T= MANE Select ENSP00000196061.4:p.Phe493=
ENST00000196061.4:c.1477T= ENSP00000196061.4:p.Phe493=
ENST00000470133.1:n.91T=
ENST00000491536.5:n.105T=
NM_000302.3:c.1477T= NP_000293.2:p.Phe493=
NM_001316320.1:c.1618T= NP_001303249.1:p.Phe540=
XM_011541594.1:c.1558T= XP_011539896.1:p.Phe520=
XM_024447707.1:c.811T= XP_024303475.1:p.Phe271=
NM_000302.4:c.1477T= MANE Select NP_000293.2:p.Phe493=
NM_001316320.2:c.1618T= NP_001303249.1:p.Phe540=