Canonical Allele Identifier: CA338424781
Gene: PLOD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11944656G>C , CM000663.2:g.11944656G>C GRCh38
NC_000001.10:g.12004713G>C , CM000663.1:g.12004713G>C GRCh37
NC_000001.9:g.11927300G>C NCBI36
NG_008159.1:g.14968G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000196061.5:c.77-3320G>C MANE Select ENSP00000196061.4:n.77-3320G>C
ENST00000196061.4:c.77-3320G>C ENSP00000196061.4:n.77-3320G>C
ENST00000358133.5:n.123-3320G>C
ENST00000429000.6:c.77-3320G>C ENSP00000405372.1:n.77-3320G>C
ENST00000449038.5:c.211G>C ENSP00000414443.1:p.Gly71Arg
ENST00000485046.5:n.120-3320G>C
NM_000302.3:c.77-3320G>C NP_000293.2:n.77-3320G>C
NM_001316320.1:c.211G>C NP_001303249.1:p.Gly71Arg
XM_011541594.1:c.151G>C XP_011539896.1:p.Gly51Arg
XM_024447707.1:c.-591+1878G>C XP_024303475.1:n.-591+1878G>C
NM_000302.4:c.77-3320G>C MANE Select NP_000293.2:n.77-3320G>C
NM_001316320.2:c.211G>C NP_001303249.1:p.Gly71Arg