Canonical Allele Identifier: CA1145930296
Gene: PLOD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11965421G= , CM000663.2:g.11965421G= GRCh38
NC_000001.10:g.12025478G= , CM000663.1:g.12025478G= GRCh37
NC_000001.9:g.11948065G= NCBI36
NG_008159.1:g.35733G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000196061.5:c.1471-59G= MANE Select ENSP00000196061.4:n.1471-59G=
ENST00000196061.4:c.1471-59G= ENSP00000196061.4:n.1471-59G=
ENST00000470133.1:n.85-59G=
ENST00000491536.5:n.99-59G=
NM_000302.3:c.1471-59G= NP_000293.2:n.1471-59G=
NM_001316320.1:c.1612-59G= NP_001303249.1:n.1612-59G=
XM_011541594.1:c.1552-59G= XP_011539896.1:n.1552-59G=
XM_024447707.1:c.805-59G= XP_024303475.1:n.805-59G=
NM_000302.4:c.1471-59G= MANE Select NP_000293.2:n.1471-59G=
NM_001316320.2:c.1612-59G= NP_001303249.1:n.1612-59G=