Canonical Allele Identifier: CA18013985
Gene: PLOD1 HGNC NCBI

Linked Data

dbSNP Id: rs71592345
gnomAD v3: 1-11965427-A-T
gnomAD v4: 1-11965427-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11965427A>T , CM000663.2:g.11965427A>T GRCh38
NC_000001.10:g.12025484A>T , CM000663.1:g.12025484A>T GRCh37
NC_000001.9:g.11948071A>T NCBI36
NG_008159.1:g.35739A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000196061.5:c.1471-53A>T MANE Select ENSP00000196061.4:n.1471-53A>T
ENST00000196061.4:c.1471-53A>T ENSP00000196061.4:n.1471-53A>T
ENST00000470133.1:n.85-53A>T
ENST00000491536.5:n.99-53A>T
NM_000302.3:c.1471-53A>T NP_000293.2:n.1471-53A>T
NM_001316320.1:c.1612-53A>T NP_001303249.1:n.1612-53A>T
XM_011541594.1:c.1552-53A>T XP_011539896.1:n.1552-53A>T
XM_024447707.1:c.805-53A>T XP_024303475.1:n.805-53A>T
NM_000302.4:c.1471-53A>T MANE Select NP_000293.2:n.1471-53A>T
NM_001316320.2:c.1612-53A>T NP_001303249.1:n.1612-53A>T