Canonical Allele Identifier: CA2493988073
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43918016T= , CM000664.2:g.43918016T= GRCh38
NC_000002.11:g.44145155T= , CM000664.1:g.44145155T= GRCh37
NC_000002.10:g.43998659T= NCBI36
NG_008247.1:g.82990A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000681993.1:n.700+9A=
ENST00000682295.1:c.303+240A= ENSP00000507499.1:n.303+240A=
ENST00000682303.1:c.*2934+9A= ENSP00000508325.1:n.*2934+9A=
ENST00000682308.1:c.3148+9A= ENSP00000507056.1:n.3148+9A=
ENST00000682480.1:c.3166+9A= ENSP00000508344.1:n.3166+9A=
ENST00000682546.1:c.3145+9A= ENSP00000508188.1:n.3145+9A=
ENST00000682585.1:c.3148+9A= ENSP00000506885.1:n.3148+9A=
ENST00000682595.1:n.3732+9A=
ENST00000682607.1:c.1566+9A=
ENST00000682779.1:c.3139+9A= ENSP00000507947.1:n.3139+9A=
ENST00000682845.1:n.2250+9A=
ENST00000682885.1:c.3103+9A= ENSP00000508036.1:n.3103+9A=
ENST00000682933.1:n.3222+9A=
ENST00000683072.1:n.3732+9A=
ENST00000683080.1:n.767+9A=
ENST00000683125.1:c.3256+9A= ENSP00000507939.1:n.3256+9A=
ENST00000683213.1:c.3151+9A= ENSP00000507751.1:n.3151+9A=
ENST00000683220.1:c.3178+9A= ENSP00000507151.1:n.3178+9A=
ENST00000683329.1:n.3951+9A=
ENST00000683346.1:c.*3023+9A= ENSP00000507458.1:n.*3023+9A=
ENST00000683409.1:n.1755+9A=
ENST00000683459.1:n.3735+9A=
ENST00000683590.1:c.2897-5458A= ENSP00000506820.1:n.2897-5458A=
ENST00000683623.1:c.3055+9A= ENSP00000507702.1:n.3055+9A=
ENST00000683645.1:n.3699+9A=
ENST00000683796.1:c.*3020+9A= ENSP00000508221.1:n.*3020+9A=
ENST00000683802.1:n.6073+9A=
ENST00000683833.1:c.3139+9A= ENSP00000506852.1:n.3139+9A=
ENST00000683994.1:c.3148+9A= ENSP00000507181.1:n.3148+9A=
ENST00000684290.1:c.*684+9A= ENSP00000507243.1:n.*684+9A=
ENST00000684306.1:c.*3061+9A= ENSP00000508384.1:n.*3061+9A=
ENST00000684341.1:n.3168+9A=
ENST00000684383.1:c.*2786+9A= ENSP00000506863.1:n.*2786+9A=
ENST00000684619.1:c.*3020+9A= ENSP00000508088.1:n.*3020+9A=
ENST00000684705.1:n.278A=
ENST00000684743.1:n.4179+9A=
ENST00000260665.12:c.3148+9A= MANE Select ENSP00000260665.7:n.3148+9A=
ENST00000260665.11:c.3148+9A= ENSP00000260665.7:n.3148+9A=
NM_133259.3:c.3148+9A= NP_573566.2:n.3148+9A=
XM_006711915.2:c.3070+9A= XP_006711978.1:n.3070+9A=
XM_006711916.2:c.3147+10A= XP_006711979.1:n.3147+10A=
XM_011532473.1:c.3148+9A= XP_011530775.1:n.3148+9A=
XM_011532474.1:c.3148+9A= XP_011530776.1:n.3148+9A=
XM_006711916.3:c.3147+10A= XP_006711979.1:n.3147+10A=
XM_017003117.1:c.3070+9A= XP_016858606.1:n.3070+9A=
XR_002958896.1:n.3190+9A=
NM_133259.4:c.3148+9A= MANE Select NP_573566.2:n.3148+9A=