Canonical Allele Identifier: CA1153865523
Gene: PLOD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11965460A= , CM000663.2:g.11965460A= GRCh38
NC_000001.10:g.12025517A= , CM000663.1:g.12025517A= GRCh37
NC_000001.9:g.11948104A= NCBI36
NG_008159.1:g.35772A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000196061.5:c.1471-20A= MANE Select ENSP00000196061.4:n.1471-20A=
ENST00000196061.4:c.1471-20A= ENSP00000196061.4:n.1471-20A=
ENST00000470133.1:n.85-20A=
ENST00000491536.5:n.99-20A=
NM_000302.3:c.1471-20A= NP_000293.2:n.1471-20A=
NM_001316320.1:c.1612-20A= NP_001303249.1:n.1612-20A=
XM_011541594.1:c.1552-20A= XP_011539896.1:n.1552-20A=
XM_024447707.1:c.805-20A= XP_024303475.1:n.805-20A=
NM_000302.4:c.1471-20A= MANE Select NP_000293.2:n.1471-20A=
NM_001316320.2:c.1612-20A= NP_001303249.1:n.1612-20A=