Canonical Allele Identifier: CA2658837026

Gene: LRPPRC

Linked Data

• gnomAD v4: 2-43918003-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43918003_43918004insA , CM000664.2:g.43918003_43918004insA	GRCh38
NC_000002.11:g.44145142_44145143insA , CM000664.1:g.44145142_44145143insA	GRCh37
NC_000002.10:g.43998646_43998647insA	NCBI36
NG_008247.1:g.83002_83003insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681993.1:n.700+21_700+22insT
ENST00000682295.1:c.303+252_303+253insT	ENSP00000507499.1:n.303+252_303+253insT
ENST00000682303.1:c.*2934+21_*2934+22insT	ENSP00000508325.1:n.*2934+21_*2934+22insT
ENST00000682308.1:c.3148+21_3148+22insT	ENSP00000507056.1:n.3148+21_3148+22insT
ENST00000682480.1:c.3166+21_3166+22insT	ENSP00000508344.1:n.3166+21_3166+22insT
ENST00000682546.1:c.3145+21_3145+22insT	ENSP00000508188.1:n.3145+21_3145+22insT
ENST00000682585.1:c.3148+21_3148+22insT	ENSP00000506885.1:n.3148+21_3148+22insT
ENST00000682595.1:n.3732+21_3732+22insT
ENST00000682607.1:c.1566+21_1566+22insT
ENST00000682779.1:c.3139+21_3139+22insT	ENSP00000507947.1:n.3139+21_3139+22insT
ENST00000682845.1:n.2250+21_2250+22insT
ENST00000682885.1:c.3103+21_3103+22insT	ENSP00000508036.1:n.3103+21_3103+22insT
ENST00000682933.1:n.3222+21_3222+22insT
ENST00000683072.1:n.3732+21_3732+22insT
ENST00000683080.1:n.767+21_767+22insT
ENST00000683125.1:c.3256+21_3256+22insT	ENSP00000507939.1:n.3256+21_3256+22insT
ENST00000683213.1:c.3151+21_3151+22insT	ENSP00000507751.1:n.3151+21_3151+22insT
ENST00000683220.1:c.3178+21_3178+22insT	ENSP00000507151.1:n.3178+21_3178+22insT
ENST00000683329.1:n.3951+21_3951+22insT
ENST00000683346.1:c.*3023+21_*3023+22insT	ENSP00000507458.1:n.*3023+21_*3023+22insT
ENST00000683409.1:n.1755+21_1755+22insT
ENST00000683459.1:n.3735+21_3735+22insT
ENST00000683590.1:c.2897-5446_2897-5445insT	ENSP00000506820.1:n.2897-5446_2897-5445insT
ENST00000683623.1:c.3055+21_3055+22insT	ENSP00000507702.1:n.3055+21_3055+22insT
ENST00000683645.1:n.3699+21_3699+22insT
ENST00000683796.1:c.*3020+21_*3020+22insT	ENSP00000508221.1:n.*3020+21_*3020+22insT
ENST00000683802.1:n.6073+21_6073+22insT
ENST00000683833.1:c.3139+21_3139+22insT	ENSP00000506852.1:n.3139+21_3139+22insT
ENST00000683994.1:c.3148+21_3148+22insT	ENSP00000507181.1:n.3148+21_3148+22insT
ENST00000684290.1:c.*684+21_*684+22insT	ENSP00000507243.1:n.*684+21_*684+22insT
ENST00000684306.1:c.*3061+21_*3061+22insT	ENSP00000508384.1:n.*3061+21_*3061+22insT
ENST00000684341.1:n.3168+21_3168+22insT
ENST00000684383.1:c.*2786+21_*2786+22insT	ENSP00000506863.1:n.*2786+21_*2786+22insT
ENST00000684619.1:c.*3020+21_*3020+22insT	ENSP00000508088.1:n.*3020+21_*3020+22insT
ENST00000684705.1:n.290_291insT
ENST00000684743.1:n.4179+21_4179+22insT
ENST00000260665.12:c.3148+21_3148+22insT MANE Select	ENSP00000260665.7:n.3148+21_3148+22insT
ENST00000260665.11:c.3148+21_3148+22insT	ENSP00000260665.7:n.3148+21_3148+22insT
NM_133259.3:c.3148+21_3148+22insT	NP_573566.2:n.3148+21_3148+22insT
XM_006711915.2:c.3070+21_3070+22insT	XP_006711978.1:n.3070+21_3070+22insT
XM_006711916.2:c.3147+22_3147+23insT	XP_006711979.1:n.3147+22_3147+23insT
XM_011532473.1:c.3148+21_3148+22insT	XP_011530775.1:n.3148+21_3148+22insT
XM_011532474.1:c.3148+21_3148+22insT	XP_011530776.1:n.3148+21_3148+22insT
XM_006711916.3:c.3147+22_3147+23insT	XP_006711979.1:n.3147+22_3147+23insT
XM_017003117.1:c.3070+21_3070+22insT	XP_016858606.1:n.3070+21_3070+22insT
XR_002958896.1:n.3190+21_3190+22insT
NM_133259.4:c.3148+21_3148+22insT MANE Select	NP_573566.2:n.3148+21_3148+22insT