Canonical Allele Identifier: CA1153866043
Gene: PLOD1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11965603G= , CM000663.2:g.11965603G= GRCh38
NC_000001.10:g.12025660G= , CM000663.1:g.12025660G= GRCh37
NC_000001.9:g.11948247G= NCBI36
NG_008159.1:g.35915G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000196061.5:c.1584+10G= MANE Select ENSP00000196061.4:n.1584+10G=
ENST00000196061.4:c.1584+10G= ENSP00000196061.4:n.1584+10G=
ENST00000470133.1:n.198+10G=
ENST00000491536.5:n.212+10G=
NM_000302.3:c.1584+10G= NP_000293.2:n.1584+10G=
NM_001316320.1:c.1725+10G= NP_001303249.1:n.1725+10G=
XM_011541594.1:c.1665+10G= XP_011539896.1:n.1665+10G=
XM_024447707.1:c.918+10G= XP_024303475.1:n.918+10G=
NM_000302.4:c.1584+10G= MANE Select NP_000293.2:n.1584+10G=
NM_001316320.2:c.1725+10G= NP_001303249.1:n.1725+10G=
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