Canonical Allele Identifier: CA2742485962
Gene: PLOD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11965463_11965465del , CM000663.2:g.11965463_11965465del GRCh38
NC_000001.10:g.12025520_12025522del , CM000663.1:g.12025520_12025522del GRCh37
NC_000001.9:g.11948107_11948109del NCBI36
NG_008159.1:g.35775_35777del

Transcript Alleles

HGVS Amino-acid Change
ENST00000196061.5:c.1471-17_1471-15del MANE Select ENSP00000196061.4:n.1471-17_1471-15del
ENST00000196061.4:c.1471-17_1471-15del ENSP00000196061.4:n.1471-17_1471-15del
ENST00000470133.1:n.85-17_85-15del
ENST00000491536.5:n.99-17_99-15del
NM_000302.3:c.1471-17_1471-15del NP_000293.2:n.1471-17_1471-15del
NM_001316320.1:c.1612-17_1612-15del NP_001303249.1:n.1612-17_1612-15del
XM_011541594.1:c.1552-17_1552-15del XP_011539896.1:n.1552-17_1552-15del
XM_024447707.1:c.805-17_805-15del XP_024303475.1:n.805-17_805-15del
NM_000302.4:c.1471-17_1471-15del MANE Select NP_000293.2:n.1471-17_1471-15del
NM_001316320.2:c.1612-17_1612-15del NP_001303249.1:n.1612-17_1612-15del