Canonical Allele Identifier: CA2658837061

Gene: LRPPRC

Linked Data

• gnomAD v4: 2-43918086-T-TGAG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43918088_43918090dup , CM000664.2:g.43918088_43918090dup	GRCh38
NC_000002.11:g.44145227_44145229dup , CM000664.1:g.44145227_44145229dup	GRCh37
NC_000002.10:g.43998731_43998733dup	NCBI36
NG_008247.1:g.82917_82919dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681993.1:n.636_638dup
ENST00000682295.1:c.303+167_303+169dup	ENSP00000507499.1:n.303+167_303+169dup
ENST00000682303.1:c.*2870_*2872dup	ENSP00000508325.1:n.*2870_*2872dup
ENST00000682308.1:c.3084_3086dup	ENSP00000507056.1:p.Ser1029_Thr1030insSer
ENST00000682480.1:c.3102_3104dup	ENSP00000508344.1:p.Ser1035_Thr1036insSer
ENST00000682546.1:c.3081_3083dup	ENSP00000508188.1:p.Ser1028_Thr1029insSer
ENST00000682585.1:c.3084_3086dup	ENSP00000506885.1:p.Ser1029_Thr1030insSer
ENST00000682595.1:n.3668_3670dup
ENST00000682607.1:c.1502_1504dup
ENST00000682779.1:c.3075_3077dup	ENSP00000507947.1:p.Ser1026_Thr1027insSer
ENST00000682845.1:n.2186_2188dup
ENST00000682885.1:c.3039_3041dup	ENSP00000508036.1:p.Ser1014_Thr1015insSer
ENST00000682933.1:n.3158_3160dup
ENST00000683072.1:n.3668_3670dup
ENST00000683080.1:n.703_705dup
ENST00000683125.1:c.3192_3194dup	ENSP00000507939.1:p.Ser1065_Thr1066insSer
ENST00000683213.1:c.3087_3089dup	ENSP00000507751.1:p.Ser1030_Thr1031insSer
ENST00000683220.1:c.3114_3116dup	ENSP00000507151.1:p.Ser1039_Thr1040insSer
ENST00000683329.1:n.3887_3889dup
ENST00000683346.1:c.*2959_*2961dup	ENSP00000507458.1:n.*2959_*2961dup
ENST00000683409.1:n.1691_1693dup
ENST00000683459.1:n.3671_3673dup
ENST00000683590.1:c.2897-5531_2897-5529dup	ENSP00000506820.1:n.2897-5531_2897-5529dup
ENST00000683623.1:c.2991_2993dup	ENSP00000507702.1:p.Ser998_Thr999insSer
ENST00000683645.1:n.3635_3637dup
ENST00000683796.1:c.*2956_*2958dup	ENSP00000508221.1:n.*2956_*2958dup
ENST00000683802.1:n.6009_6011dup
ENST00000683833.1:c.3075_3077dup	ENSP00000506852.1:p.Ser1026_Thr1027insSer
ENST00000683994.1:c.3084_3086dup	ENSP00000507181.1:p.Ser1029_Thr1030insSer
ENST00000684290.1:c.*620_*622dup	ENSP00000507243.1:n.*620_*622dup
ENST00000684306.1:c.*2997_*2999dup	ENSP00000508384.1:n.*2997_*2999dup
ENST00000684341.1:n.3104_3106dup
ENST00000684383.1:c.*2722_*2724dup	ENSP00000506863.1:n.*2722_*2724dup
ENST00000684619.1:c.*2956_*2958dup	ENSP00000508088.1:n.*2956_*2958dup
ENST00000684705.1:n.205_207dup
ENST00000684743.1:n.4115_4117dup
ENST00000260665.12:c.3084_3086dup MANE Select	ENSP00000260665.7:p.Ser1029_Thr1030insSer
ENST00000260665.11:c.3084_3086dup	ENSP00000260665.7:p.Ser1029_Thr1030insSer
NM_133259.3:c.3084_3086dup	NP_573566.2:p.Ser1029_Thr1030insSer
XM_006711915.2:c.3006_3008dup	XP_006711978.1:p.Ser1003_Thr1004insSer
XM_006711916.2:c.3084_3086dup	XP_006711979.1:p.Ser1029_Thr1030insSer
XM_011532473.1:c.3084_3086dup	XP_011530775.1:p.Ser1029_Thr1030insSer
XM_011532474.1:c.3084_3086dup	XP_011530776.1:p.Ser1029_Thr1030insSer
XM_006711916.3:c.3084_3086dup	XP_006711979.1:p.Ser1029_Thr1030insSer
XM_017003117.1:c.3006_3008dup	XP_016858606.1:p.Ser1003_Thr1004insSer
XR_002958896.1:n.3126_3128dup
NM_133259.4:c.3084_3086dup MANE Select	NP_573566.2:p.Ser1029_Thr1030insSer