Canonical Allele Identifier: CA2654777
Gene: PLOD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.146072665G>C , CM000665.2:g.146072665G>C GRCh38
NC_000003.11:g.145790452G>C , CM000665.1:g.145790452G>C GRCh37
NC_000003.10:g.147273142G>C NCBI36
NG_009251.1:g.93831C>G

Transcript Alleles

HGVS Amino-acid Change
NM_182943.3:c.1744C>G MANE Select NP_891988.1:p.Pro582Ala
ENST00000282903.10:c.1744C>G MANE Select ENSP00000282903.5:p.Pro582Ala
NM_000935.2:c.1681C>G NP_000926.2:p.Pro561Ala
NM_000935.3:c.1681C>G NP_000926.2:p.Pro561Ala
NM_182943.2:c.1744C>G NP_891988.1:p.Pro582Ala
ENST00000282903.9:c.1744C>G ENSP00000282903.5:p.Pro582Ala
ENST00000360060.7:c.1681C>G ENSP00000353170.3:p.Pro561Ala
ENST00000461497.5:c.724C>G ENSP00000419354.1:p.Pro242Ala
ENST00000469350.6:c.1597C>G ENSP00000419963.2:p.Pro533Ala
ENST00000475505.1:n.372C>G
ENST00000480704.2:c.*1508C>G ENSP00000419880.1:n.*1508C>G
ENST00000494950.5:c.1579C>G ENSP00000420094.1:p.Pro527Ala
ENST00000703517.1:n.579+30090C>G
ENST00000703518.1:c.1744C>G ENSP00000515350.1:p.Pro582Ala
ENST00000703519.1:n.1761C>G
ENST00000703520.1:c.*158C>G ENSP00000515351.1:n.*158C>G
ENST00000703521.1:c.*1096C>G ENSP00000515352.1:n.*1096C>G
ENST00000703522.1:c.1744C>G ENSP00000515353.1:p.Pro582Ala
ENST00000703523.1:c.1681C>G ENSP00000515354.1:p.Pro561Ala
ENST00000703524.1:n.1564C>G
ENST00000703525.1:n.4096C>G
ENST00000703526.1:n.1112C>G
ENST00000703527.1:c.1744C>G ENSP00000515355.1:p.Pro582Ala
ENST00000703528.1:c.1440-2571C>G ENSP00000515356.1:n.1440-2571C>G
ENST00000706626.1:c.1567C>G ENSP00000516472.1:p.Pro523Ala
ENST00000706631.1:n.2189C>G
ENST00000706632.1:n.608C>G
ENST00000706633.1:n.1579C>G
ENST00000706634.1:n.2905C>G
ENST00000706635.1:c.1576C>G ENSP00000516475.1:p.Pro526Ala
ENST00000706636.1:c.*1033C>G ENSP00000516476.1:n.*1033C>G
XM_005247535.3:c.1468C>G XP_005247592.1:p.Pro490Ala
XM_005247535.4:c.1468C>G XP_005247592.1:p.Pro490Ala
XM_017006625.2:c.1468C>G XP_016862114.1:p.Pro490Ala
XM_024453599.1:c.1405C>G XP_024309367.1:p.Pro469Ala
XR_001740176.2:n.2012C>G