Canonical Allele Identifier: CA598611
Gene: PLOD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11972858dup , CM000663.2:g.11972858dup GRCh38
NC_000001.10:g.12032915dup , CM000663.1:g.12032915dup GRCh37
NC_000001.9:g.11955502dup NCBI36
NG_008159.1:g.43170dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000196061.5:c.1903-14dup MANE Select ENSP00000196061.4:n.1903-14dup
ENST00000196061.4:c.1903-14dup ENSP00000196061.4:n.1903-14dup
ENST00000481933.1:n.1316dup
ENST00000491536.5:n.384-2425dup
NM_000302.3:c.1903-14dup NP_000293.2:n.1903-14dup
NM_001316320.1:c.2044-14dup NP_001303249.1:n.2044-14dup
XM_011541594.1:c.1984-14dup XP_011539896.1:n.1984-14dup
XM_024447707.1:c.1237-14dup XP_024303475.1:n.1237-14dup
NM_000302.4:c.1903-14dup MANE Select NP_000293.2:n.1903-14dup
NM_001316320.2:c.2044-14dup NP_001303249.1:n.2044-14dup