Canonical Allele Identifier: CA2643331200
Gene: PLOD1 HGNC NCBI

Linked Data

gnomAD v4: 1-11965439-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11965439G>A , CM000663.2:g.11965439G>A GRCh38
NC_000001.10:g.12025496G>A , CM000663.1:g.12025496G>A GRCh37
NC_000001.9:g.11948083G>A NCBI36
NG_008159.1:g.35751G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000196061.5:c.1471-41G>A MANE Select ENSP00000196061.4:n.1471-41G>A
ENST00000196061.4:c.1471-41G>A ENSP00000196061.4:n.1471-41G>A
ENST00000470133.1:n.85-41G>A
ENST00000491536.5:n.99-41G>A
NM_000302.3:c.1471-41G>A NP_000293.2:n.1471-41G>A
NM_001316320.1:c.1612-41G>A NP_001303249.1:n.1612-41G>A
XM_011541594.1:c.1552-41G>A XP_011539896.1:n.1552-41G>A
XM_024447707.1:c.805-41G>A XP_024303475.1:n.805-41G>A
NM_000302.4:c.1471-41G>A MANE Select NP_000293.2:n.1471-41G>A
NM_001316320.2:c.1612-41G>A NP_001303249.1:n.1612-41G>A