Canonical Allele Identifier: CA3071758673
Gene: PLOD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11950456A= , CM000663.2:g.11950456A= GRCh38
NC_000001.10:g.12010513A= , CM000663.1:g.12010513A= GRCh37
NC_000001.9:g.11933100A= NCBI36
NG_008159.1:g.20768A=

Transcript Alleles

HGVS Amino-acid Change
NM_000302.4:c.402A= MANE Select NP_000293.2:p.Pro134=
ENST00000196061.5:c.402A= MANE Select ENSP00000196061.4:p.Pro134=
NM_000302.3:c.402A= NP_000293.2:p.Pro134=
NM_001316320.1:c.543A= NP_001303249.1:p.Pro181=
NM_001316320.2:c.543A= NP_001303249.1:p.Pro181=
ENST00000196061.4:c.402A= ENSP00000196061.4:p.Pro134=
ENST00000358133.5:n.448A=
ENST00000429000.6:c.402A= ENSP00000405372.1:p.Pro134=
ENST00000449038.5:c.543A= ENSP00000414443.1:p.Pro181=
ENST00000485046.5:n.445A=
XM_011541594.1:c.483A= XP_011539896.1:p.Pro161=
XM_024447707.1:c.-265A= XP_024303475.1:n.-265A=