Canonical Allele Identifier: CA2493988046

Gene: LRPPRC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43917995_43917996delinsAC , CM000664.2:g.43917995_43917996delinsAC	GRCh38
NC_000002.11:g.44145134_44145135delinsAC , CM000664.1:g.44145134_44145135delinsAC	GRCh37
NC_000002.10:g.43998638_43998639delinsAC	NCBI36
NG_008247.1:g.83010_83011delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681993.1:n.700+29_700+30delinsGT
ENST00000682295.1:c.303+260_303+261delinsGT	ENSP00000507499.1:n.303+260_303+261delinsGT
ENST00000682303.1:c.*2934+29_*2934+30delinsGT	ENSP00000508325.1:n.*2934+29_*2934+30delinsGT
ENST00000682308.1:c.3148+29_3148+30delinsGT	ENSP00000507056.1:n.3148+29_3148+30delinsGT
ENST00000682480.1:c.3166+29_3166+30delinsGT	ENSP00000508344.1:n.3166+29_3166+30delinsGT
ENST00000682546.1:c.3145+29_3145+30delinsGT	ENSP00000508188.1:n.3145+29_3145+30delinsGT
ENST00000682585.1:c.3148+29_3148+30delinsGT	ENSP00000506885.1:n.3148+29_3148+30delinsGT
ENST00000682595.1:n.3732+29_3732+30delinsGT
ENST00000682607.1:c.1566+29_1566+30delinsGT
ENST00000682779.1:c.3139+29_3139+30delinsGT	ENSP00000507947.1:n.3139+29_3139+30delinsGT
ENST00000682845.1:n.2250+29_2250+30delinsGT
ENST00000682885.1:c.3103+29_3103+30delinsGT	ENSP00000508036.1:n.3103+29_3103+30delinsGT
ENST00000682933.1:n.3222+29_3222+30delinsGT
ENST00000683072.1:n.3732+29_3732+30delinsGT
ENST00000683080.1:n.767+29_767+30delinsGT
ENST00000683125.1:c.3256+29_3256+30delinsGT	ENSP00000507939.1:n.3256+29_3256+30delinsGT
ENST00000683213.1:c.3151+29_3151+30delinsGT	ENSP00000507751.1:n.3151+29_3151+30delinsGT
ENST00000683220.1:c.3178+29_3178+30delinsGT	ENSP00000507151.1:n.3178+29_3178+30delinsGT
ENST00000683329.1:n.3951+29_3951+30delinsGT
ENST00000683346.1:c.*3023+29_*3023+30delinsGT	ENSP00000507458.1:n.*3023+29_*3023+30delinsGT
ENST00000683409.1:n.1755+29_1755+30delinsGT
ENST00000683459.1:n.3735+29_3735+30delinsGT
ENST00000683590.1:c.2897-5438_2897-5437delinsGT	ENSP00000506820.1:n.2897-5438_2897-5437delinsGT
ENST00000683623.1:c.3055+29_3055+30delinsGT	ENSP00000507702.1:n.3055+29_3055+30delinsGT
ENST00000683645.1:n.3699+29_3699+30delinsGT
ENST00000683796.1:c.*3020+29_*3020+30delinsGT	ENSP00000508221.1:n.*3020+29_*3020+30delinsGT
ENST00000683802.1:n.6073+29_6073+30delinsGT
ENST00000683833.1:c.3139+29_3139+30delinsGT	ENSP00000506852.1:n.3139+29_3139+30delinsGT
ENST00000683994.1:c.3148+29_3148+30delinsGT	ENSP00000507181.1:n.3148+29_3148+30delinsGT
ENST00000684290.1:c.*684+29_*684+30delinsGT	ENSP00000507243.1:n.*684+29_*684+30delinsGT
ENST00000684306.1:c.*3061+29_*3061+30delinsGT	ENSP00000508384.1:n.*3061+29_*3061+30delinsGT
ENST00000684341.1:n.3168+29_3168+30delinsGT
ENST00000684383.1:c.*2786+29_*2786+30delinsGT	ENSP00000506863.1:n.*2786+29_*2786+30delinsGT
ENST00000684619.1:c.*3020+29_*3020+30delinsGT	ENSP00000508088.1:n.*3020+29_*3020+30delinsGT
ENST00000684705.1:n.298_299delinsGT
ENST00000684743.1:n.4179+29_4179+30delinsGT
ENST00000260665.12:c.3148+29_3148+30delinsGT MANE Select	ENSP00000260665.7:n.3148+29_3148+30delinsGT
ENST00000260665.11:c.3148+29_3148+30delinsGT	ENSP00000260665.7:n.3148+29_3148+30delinsGT
NM_133259.3:c.3148+29_3148+30delinsGT	NP_573566.2:n.3148+29_3148+30delinsGT
XM_006711915.2:c.3070+29_3070+30delinsGT	XP_006711978.1:n.3070+29_3070+30delinsGT
XM_006711916.2:c.3147+30_3147+31delinsGT	XP_006711979.1:n.3147+30_3147+31delinsGT
XM_011532473.1:c.3148+29_3148+30delinsGT	XP_011530775.1:n.3148+29_3148+30delinsGT
XM_011532474.1:c.3148+29_3148+30delinsGT	XP_011530776.1:n.3148+29_3148+30delinsGT
XM_006711916.3:c.3147+30_3147+31delinsGT	XP_006711979.1:n.3147+30_3147+31delinsGT
XM_017003117.1:c.3070+29_3070+30delinsGT	XP_016858606.1:n.3070+29_3070+30delinsGT
XR_002958896.1:n.3190+29_3190+30delinsGT
NM_133259.4:c.3148+29_3148+30delinsGT MANE Select	NP_573566.2:n.3148+29_3148+30delinsGT