Canonical Allele Identifier: CA425909259

Gene: LRPPRC

Linked Data

• MyVariant Identifiers: chr2:g.44126388G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43899249G>T , CM000664.2:g.43899249G>T	GRCh38
NC_000002.11:g.44126388G>T , CM000664.1:g.44126388G>T	GRCh37
NC_000002.10:g.43979892G>T	NCBI36
NG_008247.1:g.101757C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000419884.6:c.226C>A
ENST00000472420.6:n.874C>A
ENST00000483489.2:n.226C>A
ENST00000681993.1:n.1347C>A
ENST00000682303.1:c.*3581C>A	ENSP00000508325.1:n.*3581C>A
ENST00000682308.1:c.3795C>A	ENSP00000507056.1:p.Gly1265=
ENST00000682434.1:n.1346C>A
ENST00000682480.1:c.3813C>A	ENSP00000508344.1:p.Gly1271=
ENST00000682546.1:c.3792C>A	ENSP00000508188.1:p.Gly1264=
ENST00000682585.1:c.3795C>A	ENSP00000506885.1:p.Gly1265=
ENST00000682595.1:n.4379C>A
ENST00000682607.1:c.2213C>A
ENST00000682612.1:c.647C>A
ENST00000682779.1:c.3786C>A	ENSP00000507947.1:p.Gly1262=
ENST00000682845.1:n.2897C>A
ENST00000682885.1:c.3750C>A	ENSP00000508036.1:p.Gly1250=
ENST00000682933.1:n.3869C>A
ENST00000683002.1:c.647C>A
ENST00000683072.1:n.4379C>A
ENST00000683080.1:n.1414C>A
ENST00000683125.1:c.3903C>A	ENSP00000507939.1:p.Gly1301=
ENST00000683213.1:c.3798C>A	ENSP00000507751.1:p.Gly1266=
ENST00000683220.1:c.3825C>A	ENSP00000507151.1:p.Gly1275=
ENST00000683329.1:n.4598C>A
ENST00000683346.1:c.*3670C>A	ENSP00000507458.1:n.*3670C>A
ENST00000683409.1:n.2402C>A
ENST00000683459.1:n.4382C>A
ENST00000683528.1:c.723C>A
ENST00000683590.1:c.3543C>A	ENSP00000506820.1:p.Gly1181=
ENST00000683623.1:c.3702C>A	ENSP00000507702.1:p.Gly1234=
ENST00000683645.1:n.4346C>A
ENST00000683796.1:c.*3667C>A	ENSP00000508221.1:n.*3667C>A
ENST00000683802.1:n.6720C>A
ENST00000683833.1:c.3786C>A	ENSP00000506852.1:p.Gly1262=
ENST00000683994.1:c.3795C>A	ENSP00000507181.1:p.Gly1265=
ENST00000684290.1:c.*1331C>A	ENSP00000507243.1:n.*1331C>A
ENST00000684306.1:c.*3708C>A	ENSP00000508384.1:n.*3708C>A
ENST00000684341.1:n.3815C>A
ENST00000684383.1:c.*3433C>A	ENSP00000506863.1:n.*3433C>A
ENST00000684418.1:n.4976C>A
ENST00000684433.1:n.179C>A
ENST00000684454.1:n.3145C>A
ENST00000684619.1:c.*3667C>A	ENSP00000508088.1:n.*3667C>A
ENST00000684743.1:n.6540C>A
ENST00000260665.12:c.3795C>A MANE Select	ENSP00000260665.7:p.Gly1265=
ENST00000260665.11:c.3795C>A	ENSP00000260665.7:p.Gly1265=
ENST00000419884.5:c.36C>A	ENSP00000414207.1:p.Gly12=
ENST00000463456.5:n.2838C>A
ENST00000472420.5:n.192C>A
ENST00000483489.1:n.269C>A
NM_133259.3:c.3795C>A	NP_573566.2:p.Gly1265=
XM_006711915.2:c.3717C>A	XP_006711978.1:p.Gly1239=
XM_011532473.1:c.3795C>A	XP_011530775.1:p.Gly1265=
XM_011532474.1:c.3795C>A	XP_011530776.1:p.Gly1265=
XM_017003117.1:c.3717C>A	XP_016858606.1:p.Gly1239=
XR_002958896.1:n.3837C>A
NM_133259.4:c.3795C>A MANE Select	NP_573566.2:p.Gly1265=