Canonical Allele Identifier: CA2654683

Gene: PLOD2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.146071057C>G , CM000665.2:g.146071057C>G	GRCh38
NC_000003.11:g.145788844C>G , CM000665.1:g.145788844C>G	GRCh37
NC_000003.10:g.147271534C>G	NCBI36
NG_009251.1:g.95439G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000469350.6:c.1959G>C	ENSP00000419963.2:p.Val653=
ENST00000480704.2:c.*1870G>C	ENSP00000419880.1:n.*1870G>C
ENST00000703517.1:n.579+31698G>C
ENST00000703518.1:c.2106G>C	ENSP00000515350.1:p.Val702=
ENST00000703519.1:n.2123G>C
ENST00000703520.1:c.*520G>C	ENSP00000515351.1:n.*520G>C
ENST00000703521.1:c.*1458G>C	ENSP00000515352.1:n.*1458G>C
ENST00000703522.1:c.2106G>C	ENSP00000515353.1:p.Val702=
ENST00000703523.1:c.2043G>C	ENSP00000515354.1:p.Val681=
ENST00000703524.1:n.1956G>C
ENST00000703525.1:n.4458G>C
ENST00000703526.1:n.1474G>C
ENST00000703527.1:c.2106G>C	ENSP00000515355.1:p.Val702=
ENST00000703528.1:c.1440-963G>C	ENSP00000515356.1:n.1440-963G>C
ENST00000706626.1:c.1929G>C	ENSP00000516472.1:p.Val643=
ENST00000706631.1:n.2551G>C
ENST00000706632.1:n.970G>C
ENST00000706633.1:n.3078G>C
ENST00000706634.1:n.3267G>C
ENST00000706635.1:c.1938G>C	ENSP00000516475.1:p.Val646=
ENST00000706636.1:c.*1395G>C	ENSP00000516476.1:n.*1395G>C
ENST00000282903.10:c.2106G>C MANE Select	ENSP00000282903.5:p.Val702=
ENST00000282903.9:c.2106G>C	ENSP00000282903.5:p.Val702=
ENST00000360060.7:c.2043G>C	ENSP00000353170.3:p.Val681=
ENST00000461497.5:c.1086G>C	ENSP00000419354.1:p.Val362=
ENST00000494950.5:c.1941G>C	ENSP00000420094.1:p.Val647=
ENST00000495700.1:n.114G>C
NM_000935.2:c.2043G>C	NP_000926.2:p.Val681=
NM_182943.2:c.2106G>C	NP_891988.1:p.Val702=
XM_005247535.3:c.1830G>C	XP_005247592.1:p.Val610=
XM_005247535.4:c.1830G>C	XP_005247592.1:p.Val610=
XM_017006625.2:c.1830G>C	XP_016862114.1:p.Val610=
XM_024453599.1:c.1767G>C	XP_024309367.1:p.Val589=
XR_001740176.2:n.2374G>C
NM_182943.3:c.2106G>C MANE Select	NP_891988.1:p.Val702=
NM_000935.3:c.2043G>C	NP_000926.2:p.Val681=