Canonical Allele Identifier: CA1153866354
Gene: PLOD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11965651T= , CM000663.2:g.11965651T= GRCh38
NC_000001.10:g.12025708T= , CM000663.1:g.12025708T= GRCh37
NC_000001.9:g.11948295T= NCBI36
NG_008159.1:g.35963T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000196061.5:c.1584+58T= MANE Select ENSP00000196061.4:n.1584+58T=
ENST00000196061.4:c.1584+58T= ENSP00000196061.4:n.1584+58T=
ENST00000470133.1:n.198+58T=
ENST00000491536.5:n.212+58T=
NM_000302.3:c.1584+58T= NP_000293.2:n.1584+58T=
NM_001316320.1:c.1725+58T= NP_001303249.1:n.1725+58T=
XM_011541594.1:c.1665+58T= XP_011539896.1:n.1665+58T=
XM_024447707.1:c.918+58T= XP_024303475.1:n.918+58T=
NM_000302.4:c.1584+58T= MANE Select NP_000293.2:n.1584+58T=
NM_001316320.2:c.1725+58T= NP_001303249.1:n.1725+58T=