Canonical Allele Identifier: CA2493988065

Gene: LRPPRC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43918008_43918009delinsTC , CM000664.2:g.43918008_43918009delinsTC	GRCh38
NC_000002.11:g.44145147_44145148delinsTC , CM000664.1:g.44145147_44145148delinsTC	GRCh37
NC_000002.10:g.43998651_43998652delinsTC	NCBI36
NG_008247.1:g.82997_82998delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681993.1:n.700+16_700+17delinsGA
ENST00000682295.1:c.303+247_303+248delinsGA	ENSP00000507499.1:n.303+247_303+248delinsGA
ENST00000682303.1:c.*2934+16_*2934+17delinsGA	ENSP00000508325.1:n.*2934+16_*2934+17delinsGA
ENST00000682308.1:c.3148+16_3148+17delinsGA	ENSP00000507056.1:n.3148+16_3148+17delinsGA
ENST00000682480.1:c.3166+16_3166+17delinsGA	ENSP00000508344.1:n.3166+16_3166+17delinsGA
ENST00000682546.1:c.3145+16_3145+17delinsGA	ENSP00000508188.1:n.3145+16_3145+17delinsGA
ENST00000682585.1:c.3148+16_3148+17delinsGA	ENSP00000506885.1:n.3148+16_3148+17delinsGA
ENST00000682595.1:n.3732+16_3732+17delinsGA
ENST00000682607.1:c.1566+16_1566+17delinsGA
ENST00000682779.1:c.3139+16_3139+17delinsGA	ENSP00000507947.1:n.3139+16_3139+17delinsGA
ENST00000682845.1:n.2250+16_2250+17delinsGA
ENST00000682885.1:c.3103+16_3103+17delinsGA	ENSP00000508036.1:n.3103+16_3103+17delinsGA
ENST00000682933.1:n.3222+16_3222+17delinsGA
ENST00000683072.1:n.3732+16_3732+17delinsGA
ENST00000683080.1:n.767+16_767+17delinsGA
ENST00000683125.1:c.3256+16_3256+17delinsGA	ENSP00000507939.1:n.3256+16_3256+17delinsGA
ENST00000683213.1:c.3151+16_3151+17delinsGA	ENSP00000507751.1:n.3151+16_3151+17delinsGA
ENST00000683220.1:c.3178+16_3178+17delinsGA	ENSP00000507151.1:n.3178+16_3178+17delinsGA
ENST00000683329.1:n.3951+16_3951+17delinsGA
ENST00000683346.1:c.*3023+16_*3023+17delinsGA	ENSP00000507458.1:n.*3023+16_*3023+17delinsGA
ENST00000683409.1:n.1755+16_1755+17delinsGA
ENST00000683459.1:n.3735+16_3735+17delinsGA
ENST00000683590.1:c.2897-5451_2897-5450delinsGA	ENSP00000506820.1:n.2897-5451_2897-5450delinsGA
ENST00000683623.1:c.3055+16_3055+17delinsGA	ENSP00000507702.1:n.3055+16_3055+17delinsGA
ENST00000683645.1:n.3699+16_3699+17delinsGA
ENST00000683796.1:c.*3020+16_*3020+17delinsGA	ENSP00000508221.1:n.*3020+16_*3020+17delinsGA
ENST00000683802.1:n.6073+16_6073+17delinsGA
ENST00000683833.1:c.3139+16_3139+17delinsGA	ENSP00000506852.1:n.3139+16_3139+17delinsGA
ENST00000683994.1:c.3148+16_3148+17delinsGA	ENSP00000507181.1:n.3148+16_3148+17delinsGA
ENST00000684290.1:c.*684+16_*684+17delinsGA	ENSP00000507243.1:n.*684+16_*684+17delinsGA
ENST00000684306.1:c.*3061+16_*3061+17delinsGA	ENSP00000508384.1:n.*3061+16_*3061+17delinsGA
ENST00000684341.1:n.3168+16_3168+17delinsGA
ENST00000684383.1:c.*2786+16_*2786+17delinsGA	ENSP00000506863.1:n.*2786+16_*2786+17delinsGA
ENST00000684619.1:c.*3020+16_*3020+17delinsGA	ENSP00000508088.1:n.*3020+16_*3020+17delinsGA
ENST00000684705.1:n.285_286delinsGA
ENST00000684743.1:n.4179+16_4179+17delinsGA
ENST00000260665.12:c.3148+16_3148+17delinsGA MANE Select	ENSP00000260665.7:n.3148+16_3148+17delinsGA
ENST00000260665.11:c.3148+16_3148+17delinsGA	ENSP00000260665.7:n.3148+16_3148+17delinsGA
NM_133259.3:c.3148+16_3148+17delinsGA	NP_573566.2:n.3148+16_3148+17delinsGA
XM_006711915.2:c.3070+16_3070+17delinsGA	XP_006711978.1:n.3070+16_3070+17delinsGA
XM_006711916.2:c.3147+17_3147+18delinsGA	XP_006711979.1:n.3147+17_3147+18delinsGA
XM_011532473.1:c.3148+16_3148+17delinsGA	XP_011530775.1:n.3148+16_3148+17delinsGA
XM_011532474.1:c.3148+16_3148+17delinsGA	XP_011530776.1:n.3148+16_3148+17delinsGA
XM_006711916.3:c.3147+17_3147+18delinsGA	XP_006711979.1:n.3147+17_3147+18delinsGA
XM_017003117.1:c.3070+16_3070+17delinsGA	XP_016858606.1:n.3070+16_3070+17delinsGA
XR_002958896.1:n.3190+16_3190+17delinsGA
NM_133259.4:c.3148+16_3148+17delinsGA MANE Select	NP_573566.2:n.3148+16_3148+17delinsGA