Canonical Allele Identifier: CA2655104

Gene: PLOD2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.146091818G>A , CM000665.2:g.146091818G>A	GRCh38
NC_000003.11:g.145809605G>A , CM000665.1:g.145809605G>A	GRCh37
NC_000003.10:g.147292295G>A	NCBI36
NG_009251.1:g.74678C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000469350.6:c.777C>T	ENSP00000419963.2:p.Val259=
ENST00000480704.2:c.*625C>T	ENSP00000419880.1:n.*625C>T
ENST00000703517.1:n.579+10937C>T
ENST00000703518.1:c.861C>T	ENSP00000515350.1:p.Val287=
ENST00000703519.1:n.878C>T
ENST00000703520.1:c.861C>T	ENSP00000515351.1:p.Val287=
ENST00000703521.1:c.*213C>T	ENSP00000515352.1:n.*213C>T
ENST00000703522.1:c.861C>T	ENSP00000515353.1:p.Val287=
ENST00000703523.1:c.861C>T	ENSP00000515354.1:p.Val287=
ENST00000703524.1:n.384C>T
ENST00000703525.1:n.1056C>T
ENST00000703526.1:n.229C>T
ENST00000703527.1:c.861C>T	ENSP00000515355.1:p.Val287=
ENST00000703528.1:c.696C>T	ENSP00000515356.1:p.Val232=
ENST00000703529.1:n.1056C>T
ENST00000706626.1:c.861C>T	ENSP00000516472.1:p.Val287=
ENST00000706627.1:n.1056C>T
ENST00000706634.1:n.1056C>T
ENST00000706635.1:c.861C>T	ENSP00000516475.1:p.Val287=
ENST00000706636.1:c.*213C>T	ENSP00000516476.1:n.*213C>T
ENST00000282903.10:c.861C>T MANE Select	ENSP00000282903.5:p.Val287=
ENST00000282903.9:c.861C>T	ENSP00000282903.5:p.Val287=
ENST00000360060.7:c.861C>T	ENSP00000353170.3:p.Val287=
ENST00000494950.5:c.696C>T	ENSP00000420094.1:p.Val232=
NM_000935.2:c.861C>T	NP_000926.2:p.Val287=
NM_182943.2:c.861C>T	NP_891988.1:p.Val287=
XM_005247535.3:c.585C>T	XP_005247592.1:p.Val195=
XM_005247536.3:c.861C>T	XP_005247593.1:p.Val287=
XM_005247535.4:c.585C>T	XP_005247592.1:p.Val195=
XM_017006625.2:c.585C>T	XP_016862114.1:p.Val195=
XM_024453599.1:c.585C>T	XP_024309367.1:p.Val195=
XR_001740176.2:n.1056C>T
NM_182943.3:c.861C>T MANE Select	NP_891988.1:p.Val287=
NM_000935.3:c.861C>T	NP_000926.2:p.Val287=