Canonical Allele Identifier: CA2493988044

Gene: LRPPRC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43917993_43917995delinsCCA , CM000664.2:g.43917993_43917995delinsCCA	GRCh38
NC_000002.11:g.44145132_44145134delinsCCA , CM000664.1:g.44145132_44145134delinsCCA	GRCh37
NC_000002.10:g.43998636_43998638delinsCCA	NCBI36
NG_008247.1:g.83011_83013delinsTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681993.1:n.700+30_700+32delinsTGG
ENST00000682295.1:c.303+261_303+263delinsTGG	ENSP00000507499.1:n.303+261_303+263delinsTGG
ENST00000682303.1:c.*2934+30_*2934+32delinsTGG	ENSP00000508325.1:n.*2934+30_*2934+32delinsTGG
ENST00000682308.1:c.3148+30_3148+32delinsTGG	ENSP00000507056.1:n.3148+30_3148+32delinsTGG
ENST00000682480.1:c.3166+30_3166+32delinsTGG	ENSP00000508344.1:n.3166+30_3166+32delinsTGG
ENST00000682546.1:c.3145+30_3145+32delinsTGG	ENSP00000508188.1:n.3145+30_3145+32delinsTGG
ENST00000682585.1:c.3148+30_3148+32delinsTGG	ENSP00000506885.1:n.3148+30_3148+32delinsTGG
ENST00000682595.1:n.3732+30_3732+32delinsTGG
ENST00000682607.1:c.1566+30_1566+32delinsTGG
ENST00000682779.1:c.3139+30_3139+32delinsTGG	ENSP00000507947.1:n.3139+30_3139+32delinsTGG
ENST00000682845.1:n.2250+30_2250+32delinsTGG
ENST00000682885.1:c.3103+30_3103+32delinsTGG	ENSP00000508036.1:n.3103+30_3103+32delinsTGG
ENST00000682933.1:n.3222+30_3222+32delinsTGG
ENST00000683072.1:n.3732+30_3732+32delinsTGG
ENST00000683080.1:n.767+30_767+32delinsTGG
ENST00000683125.1:c.3256+30_3256+32delinsTGG	ENSP00000507939.1:n.3256+30_3256+32delinsTGG
ENST00000683213.1:c.3151+30_3151+32delinsTGG	ENSP00000507751.1:n.3151+30_3151+32delinsTGG
ENST00000683220.1:c.3178+30_3178+32delinsTGG	ENSP00000507151.1:n.3178+30_3178+32delinsTGG
ENST00000683329.1:n.3951+30_3951+32delinsTGG
ENST00000683346.1:c.*3023+30_*3023+32delinsTGG	ENSP00000507458.1:n.*3023+30_*3023+32delinsTGG
ENST00000683409.1:n.1755+30_1755+32delinsTGG
ENST00000683459.1:n.3735+30_3735+32delinsTGG
ENST00000683590.1:c.2897-5437_2897-5435delinsTGG	ENSP00000506820.1:n.2897-5437_2897-5435delinsTGG
ENST00000683623.1:c.3055+30_3055+32delinsTGG	ENSP00000507702.1:n.3055+30_3055+32delinsTGG
ENST00000683645.1:n.3699+30_3699+32delinsTGG
ENST00000683796.1:c.*3020+30_*3020+32delinsTGG	ENSP00000508221.1:n.*3020+30_*3020+32delinsTGG
ENST00000683802.1:n.6073+30_6073+32delinsTGG
ENST00000683833.1:c.3139+30_3139+32delinsTGG	ENSP00000506852.1:n.3139+30_3139+32delinsTGG
ENST00000683994.1:c.3148+30_3148+32delinsTGG	ENSP00000507181.1:n.3148+30_3148+32delinsTGG
ENST00000684290.1:c.*684+30_*684+32delinsTGG	ENSP00000507243.1:n.*684+30_*684+32delinsTGG
ENST00000684306.1:c.*3061+30_*3061+32delinsTGG	ENSP00000508384.1:n.*3061+30_*3061+32delinsTGG
ENST00000684341.1:n.3168+30_3168+32delinsTGG
ENST00000684383.1:c.*2786+30_*2786+32delinsTGG	ENSP00000506863.1:n.*2786+30_*2786+32delinsTGG
ENST00000684619.1:c.*3020+30_*3020+32delinsTGG	ENSP00000508088.1:n.*3020+30_*3020+32delinsTGG
ENST00000684705.1:n.299_301delinsTGG
ENST00000684743.1:n.4179+30_4179+32delinsTGG
ENST00000260665.12:c.3148+30_3148+32delinsTGG MANE Select	ENSP00000260665.7:n.3148+30_3148+32delinsTGG
ENST00000260665.11:c.3148+30_3148+32delinsTGG	ENSP00000260665.7:n.3148+30_3148+32delinsTGG
NM_133259.3:c.3148+30_3148+32delinsTGG	NP_573566.2:n.3148+30_3148+32delinsTGG
XM_006711915.2:c.3070+30_3070+32delinsTGG	XP_006711978.1:n.3070+30_3070+32delinsTGG
XM_006711916.2:c.3147+31_3147+33delinsTGG	XP_006711979.1:n.3147+31_3147+33delinsTGG
XM_011532473.1:c.3148+30_3148+32delinsTGG	XP_011530775.1:n.3148+30_3148+32delinsTGG
XM_011532474.1:c.3148+30_3148+32delinsTGG	XP_011530776.1:n.3148+30_3148+32delinsTGG
XM_006711916.3:c.3147+31_3147+33delinsTGG	XP_006711979.1:n.3147+31_3147+33delinsTGG
XM_017003117.1:c.3070+30_3070+32delinsTGG	XP_016858606.1:n.3070+30_3070+32delinsTGG
XR_002958896.1:n.3190+30_3190+32delinsTGG
NM_133259.4:c.3148+30_3148+32delinsTGG MANE Select	NP_573566.2:n.3148+30_3148+32delinsTGG