Canonical Allele Identifier: CA1153865560
Gene: PLOD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11965471_11965472delinsCC , CM000663.2:g.11965471_11965472delinsCC GRCh38
NC_000001.10:g.12025528_12025529delinsCC , CM000663.1:g.12025528_12025529delinsCC GRCh37
NC_000001.9:g.11948115_11948116delinsCC NCBI36
NG_008159.1:g.35783_35784delinsCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000196061.5:c.1471-9_1471-8delinsCC MANE Select ENSP00000196061.4:n.1471-9_1471-8delinsCC
ENST00000196061.4:c.1471-9_1471-8delinsCC ENSP00000196061.4:n.1471-9_1471-8delinsCC
ENST00000470133.1:n.85-9_85-8delinsCC
ENST00000491536.5:n.99-9_99-8delinsCC
NM_000302.3:c.1471-9_1471-8delinsCC NP_000293.2:n.1471-9_1471-8delinsCC
NM_001316320.1:c.1612-9_1612-8delinsCC NP_001303249.1:n.1612-9_1612-8delinsCC
XM_011541594.1:c.1552-9_1552-8delinsCC XP_011539896.1:n.1552-9_1552-8delinsCC
XM_024447707.1:c.805-9_805-8delinsCC XP_024303475.1:n.805-9_805-8delinsCC
NM_000302.4:c.1471-9_1471-8delinsCC MANE Select NP_000293.2:n.1471-9_1471-8delinsCC
NM_001316320.2:c.1612-9_1612-8delinsCC NP_001303249.1:n.1612-9_1612-8delinsCC