Canonical Allele Identifier: CA1153865822
Gene: PLOD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11965553A= , CM000663.2:g.11965553A= GRCh38
NC_000001.10:g.12025610A= , CM000663.1:g.12025610A= GRCh37
NC_000001.9:g.11948197A= NCBI36
NG_008159.1:g.35865A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000196061.5:c.1544A= MANE Select ENSP00000196061.4:p.His515=
ENST00000196061.4:c.1544A= ENSP00000196061.4:p.His515=
ENST00000470133.1:n.158A=
ENST00000491536.5:n.172A=
NM_000302.3:c.1544A= NP_000293.2:p.His515=
NM_001316320.1:c.1685A= NP_001303249.1:p.His562=
XM_011541594.1:c.1625A= XP_011539896.1:p.His542=
XM_024447707.1:c.878A= XP_024303475.1:p.His293=
NM_000302.4:c.1544A= MANE Select NP_000293.2:p.His515=
NM_001316320.2:c.1685A= NP_001303249.1:p.His562=