Canonical Allele Identifier: CA354883639

Gene: PLOD2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.146071417G>C , CM000665.2:g.146071417G>C	GRCh38
NC_000003.11:g.145789204G>C , CM000665.1:g.145789204G>C	GRCh37
NC_000003.10:g.147271894G>C	NCBI36
NG_009251.1:g.95079C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000469350.6:c.1708C>G	ENSP00000419963.2:p.Arg570Gly
ENST00000480704.2:c.*1619C>G	ENSP00000419880.1:n.*1619C>G
ENST00000703517.1:n.579+31338C>G
ENST00000703518.1:c.1855C>G	ENSP00000515350.1:p.Arg619Gly
ENST00000703519.1:n.1872C>G
ENST00000703520.1:c.*269C>G	ENSP00000515351.1:n.*269C>G
ENST00000703521.1:c.*1207C>G	ENSP00000515352.1:n.*1207C>G
ENST00000703522.1:c.1855C>G	ENSP00000515353.1:p.Arg619Gly
ENST00000703523.1:c.1792C>G	ENSP00000515354.1:p.Arg598Gly
ENST00000703524.1:n.1675C>G
ENST00000703525.1:n.4207C>G
ENST00000703526.1:n.1223C>G
ENST00000703527.1:c.1855C>G	ENSP00000515355.1:p.Arg619Gly
ENST00000703528.1:c.1440-1323C>G	ENSP00000515356.1:n.1440-1323C>G
ENST00000706626.1:c.1678C>G	ENSP00000516472.1:p.Arg560Gly
ENST00000706631.1:n.2300C>G
ENST00000706632.1:n.719C>G
ENST00000706633.1:n.2827C>G
ENST00000706634.1:n.3016C>G
ENST00000706635.1:c.1687C>G	ENSP00000516475.1:p.Arg563Gly
ENST00000706636.1:c.*1144C>G	ENSP00000516476.1:n.*1144C>G
ENST00000282903.10:c.1855C>G MANE Select	ENSP00000282903.5:p.Arg619Gly
ENST00000282903.9:c.1855C>G	ENSP00000282903.5:p.Arg619Gly
ENST00000360060.7:c.1792C>G	ENSP00000353170.3:p.Arg598Gly
ENST00000461497.5:c.835C>G	ENSP00000419354.1:p.Arg279Gly
ENST00000494950.5:c.1690C>G	ENSP00000420094.1:p.Arg564Gly
NM_000935.2:c.1792C>G	NP_000926.2:p.Arg598Gly
NM_182943.2:c.1855C>G	NP_891988.1:p.Arg619Gly
XM_005247535.3:c.1579C>G	XP_005247592.1:p.Arg527Gly
XM_005247535.4:c.1579C>G	XP_005247592.1:p.Arg527Gly
XM_017006625.2:c.1579C>G	XP_016862114.1:p.Arg527Gly
XM_024453599.1:c.1516C>G	XP_024309367.1:p.Arg506Gly
XR_001740176.2:n.2123C>G
NM_182943.3:c.1855C>G MANE Select	NP_891988.1:p.Arg619Gly
NM_000935.3:c.1792C>G	NP_000926.2:p.Arg598Gly