Canonical Allele Identifier: CA2493977927
Gene: LRPPRC HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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