Canonical Allele Identifier: CA1153865336
Gene: PLOD1 HGNC NCBI

Linked Data

dbSNP Id: rs1645808729

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11965387C>T , CM000663.2:g.11965387C>T GRCh38
NC_000001.10:g.12025444C>T , CM000663.1:g.12025444C>T GRCh37
NC_000001.9:g.11948031C>T NCBI36
NG_008159.1:g.35699C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000196061.5:c.1471-93C>T MANE Select ENSP00000196061.4:n.1471-93C>T
ENST00000196061.4:c.1471-93C>T ENSP00000196061.4:n.1471-93C>T
ENST00000470133.1:n.85-93C>T
ENST00000491536.5:n.99-93C>T
NM_000302.3:c.1471-93C>T NP_000293.2:n.1471-93C>T
NM_001316320.1:c.1612-93C>T NP_001303249.1:n.1612-93C>T
XM_011541594.1:c.1552-93C>T XP_011539896.1:n.1552-93C>T
XM_024447707.1:c.805-93C>T XP_024303475.1:n.805-93C>T
NM_000302.4:c.1471-93C>T MANE Select NP_000293.2:n.1471-93C>T
NM_001316320.2:c.1612-93C>T NP_001303249.1:n.1612-93C>T