Canonical Allele Identifier: CA2493988178

Gene: LRPPRC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43918243_43918244delinsCA , CM000664.2:g.43918243_43918244delinsCA	GRCh38
NC_000002.11:g.44145382_44145383delinsCA , CM000664.1:g.44145382_44145383delinsCA	GRCh37
NC_000002.10:g.43998886_43998887delinsCA	NCBI36
NG_008247.1:g.82762_82763delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681993.1:n.591+12_591+13delinsTG
ENST00000682295.1:c.303+12_303+13delinsTG	ENSP00000507499.1:n.303+12_303+13delinsTG
ENST00000682303.1:c.*2825+12_*2825+13delinsTG	ENSP00000508325.1:n.*2825+12_*2825+13delinsTG
ENST00000682308.1:c.3039+12_3039+13delinsTG	ENSP00000507056.1:n.3039+12_3039+13delinsTG
ENST00000682480.1:c.3039+12_3039+13delinsTG	ENSP00000508344.1:n.3039+12_3039+13delinsTG
ENST00000682546.1:c.3036+12_3036+13delinsTG	ENSP00000508188.1:n.3036+12_3036+13delinsTG
ENST00000682585.1:c.3039+12_3039+13delinsTG	ENSP00000506885.1:n.3039+12_3039+13delinsTG
ENST00000682595.1:n.3623+12_3623+13delinsTG
ENST00000682607.1:c.1457+12_1457+13delinsTG
ENST00000682779.1:c.3030+12_3030+13delinsTG	ENSP00000507947.1:n.3030+12_3030+13delinsTG
ENST00000682845.1:n.2141+12_2141+13delinsTG
ENST00000682885.1:c.2994+12_2994+13delinsTG	ENSP00000508036.1:n.2994+12_2994+13delinsTG
ENST00000682933.1:n.3113+12_3113+13delinsTG
ENST00000683072.1:n.3623+12_3623+13delinsTG
ENST00000683080.1:n.658+12_658+13delinsTG
ENST00000683125.1:c.3147+12_3147+13delinsTG	ENSP00000507939.1:n.3147+12_3147+13delinsTG
ENST00000683213.1:c.3042+12_3042+13delinsTG	ENSP00000507751.1:n.3042+12_3042+13delinsTG
ENST00000683220.1:c.3069+12_3069+13delinsTG	ENSP00000507151.1:n.3069+12_3069+13delinsTG
ENST00000683329.1:n.3842+12_3842+13delinsTG
ENST00000683346.1:c.*2914+12_*2914+13delinsTG	ENSP00000507458.1:n.*2914+12_*2914+13delinsTG
ENST00000683409.1:n.1646+12_1646+13delinsTG
ENST00000683459.1:n.3626+12_3626+13delinsTG
ENST00000683590.1:c.2897-5686_2897-5685delinsTG	ENSP00000506820.1:n.2897-5686_2897-5685delinsTG
ENST00000683623.1:c.2946+12_2946+13delinsTG	ENSP00000507702.1:n.2946+12_2946+13delinsTG
ENST00000683645.1:n.3590+12_3590+13delinsTG
ENST00000683796.1:c.*2911+12_*2911+13delinsTG	ENSP00000508221.1:n.*2911+12_*2911+13delinsTG
ENST00000683802.1:n.5964+12_5964+13delinsTG
ENST00000683833.1:c.3030+12_3030+13delinsTG	ENSP00000506852.1:n.3030+12_3030+13delinsTG
ENST00000683994.1:c.3039+12_3039+13delinsTG	ENSP00000507181.1:n.3039+12_3039+13delinsTG
ENST00000684290.1:c.*575+12_*575+13delinsTG	ENSP00000507243.1:n.*575+12_*575+13delinsTG
ENST00000684306.1:c.*2952+12_*2952+13delinsTG	ENSP00000508384.1:n.*2952+12_*2952+13delinsTG
ENST00000684341.1:n.3059+12_3059+13delinsTG
ENST00000684383.1:c.*2677+12_*2677+13delinsTG	ENSP00000506863.1:n.*2677+12_*2677+13delinsTG
ENST00000684619.1:c.*2911+12_*2911+13delinsTG	ENSP00000508088.1:n.*2911+12_*2911+13delinsTG
ENST00000684705.1:n.160+12_160+13delinsTG
ENST00000684743.1:n.4070+12_4070+13delinsTG
ENST00000260665.12:c.3039+12_3039+13delinsTG MANE Select	ENSP00000260665.7:n.3039+12_3039+13delinsTG
ENST00000260665.11:c.3039+12_3039+13delinsTG	ENSP00000260665.7:n.3039+12_3039+13delinsTG
NM_133259.3:c.3039+12_3039+13delinsTG	NP_573566.2:n.3039+12_3039+13delinsTG
XM_006711915.2:c.2961+12_2961+13delinsTG	XP_006711978.1:n.2961+12_2961+13delinsTG
XM_006711916.2:c.3039+12_3039+13delinsTG	XP_006711979.1:n.3039+12_3039+13delinsTG
XM_011532473.1:c.3039+12_3039+13delinsTG	XP_011530775.1:n.3039+12_3039+13delinsTG
XM_011532474.1:c.3039+12_3039+13delinsTG	XP_011530776.1:n.3039+12_3039+13delinsTG
XM_006711916.3:c.3039+12_3039+13delinsTG	XP_006711979.1:n.3039+12_3039+13delinsTG
XM_017003117.1:c.2961+12_2961+13delinsTG	XP_016858606.1:n.2961+12_2961+13delinsTG
XR_002958896.1:n.3081+12_3081+13delinsTG
NM_133259.4:c.3039+12_3039+13delinsTG MANE Select	NP_573566.2:n.3039+12_3039+13delinsTG