Canonical Allele Identifier: CA2654778

Gene: PLOD2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.146072676T>C , CM000665.2:g.146072676T>C	GRCh38
NC_000003.11:g.145790463T>C , CM000665.1:g.145790463T>C	GRCh37
NC_000003.10:g.147273153T>C	NCBI36
NG_009251.1:g.93820A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_182943.3:c.1744-11A>G MANE Select	NP_891988.1:n.1744-11A>G
ENST00000282903.10:c.1744-11A>G MANE Select	ENSP00000282903.5:n.1744-11A>G
NM_000935.2:c.1681-11A>G	NP_000926.2:n.1681-11A>G
NM_000935.3:c.1681-11A>G	NP_000926.2:n.1681-11A>G
NM_182943.2:c.1744-11A>G	NP_891988.1:n.1744-11A>G
ENST00000282903.9:c.1744-11A>G	ENSP00000282903.5:n.1744-11A>G
ENST00000360060.7:c.1681-11A>G	ENSP00000353170.3:n.1681-11A>G
ENST00000461497.5:c.724-11A>G	ENSP00000419354.1:n.724-11A>G
ENST00000469350.6:c.1597-11A>G	ENSP00000419963.2:n.1597-11A>G
ENST00000475505.1:n.372-11A>G
ENST00000480704.2:c.*1508-11A>G	ENSP00000419880.1:n.*1508-11A>G
ENST00000494950.5:c.1579-11A>G	ENSP00000420094.1:n.1579-11A>G
ENST00000703517.1:n.579+30079A>G
ENST00000703518.1:c.1744-11A>G	ENSP00000515350.1:n.1744-11A>G
ENST00000703519.1:n.1761-11A>G
ENST00000703520.1:c.*158-11A>G	ENSP00000515351.1:n.*158-11A>G
ENST00000703521.1:c.*1096-11A>G	ENSP00000515352.1:n.*1096-11A>G
ENST00000703522.1:c.1744-11A>G	ENSP00000515353.1:n.1744-11A>G
ENST00000703523.1:c.1681-11A>G	ENSP00000515354.1:n.1681-11A>G
ENST00000703524.1:n.1564-11A>G
ENST00000703525.1:n.4096-11A>G
ENST00000703526.1:n.1112-11A>G
ENST00000703527.1:c.1744-11A>G	ENSP00000515355.1:n.1744-11A>G
ENST00000703528.1:c.1440-2582A>G	ENSP00000515356.1:n.1440-2582A>G
ENST00000706626.1:c.1567-11A>G	ENSP00000516472.1:n.1567-11A>G
ENST00000706631.1:n.2189-11A>G
ENST00000706632.1:n.608-11A>G
ENST00000706633.1:n.1568A>G
ENST00000706634.1:n.2905-11A>G
ENST00000706635.1:c.1576-11A>G	ENSP00000516475.1:n.1576-11A>G
ENST00000706636.1:c.*1033-11A>G	ENSP00000516476.1:n.*1033-11A>G
XM_005247535.3:c.1468-11A>G	XP_005247592.1:n.1468-11A>G
XM_005247535.4:c.1468-11A>G	XP_005247592.1:n.1468-11A>G
XM_017006625.2:c.1468-11A>G	XP_016862114.1:n.1468-11A>G
XM_024453599.1:c.1405-11A>G	XP_024309367.1:n.1405-11A>G
XR_001740176.2:n.2012-11A>G