Canonical Allele Identifier: CA2493988007
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43917928T= , CM000664.2:g.43917928T= GRCh38
NC_000002.11:g.44145067T= , CM000664.1:g.44145067T= GRCh37
NC_000002.10:g.43998571T= NCBI36
NG_008247.1:g.83078A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000681993.1:n.700+97A=
ENST00000682295.1:c.303+328A= ENSP00000507499.1:n.303+328A=
ENST00000682303.1:c.*2934+97A= ENSP00000508325.1:n.*2934+97A=
ENST00000682308.1:c.3148+97A= ENSP00000507056.1:n.3148+97A=
ENST00000682480.1:c.3166+97A= ENSP00000508344.1:n.3166+97A=
ENST00000682546.1:c.3145+97A= ENSP00000508188.1:n.3145+97A=
ENST00000682585.1:c.3148+97A= ENSP00000506885.1:n.3148+97A=
ENST00000682595.1:n.3732+97A=
ENST00000682607.1:c.1566+97A=
ENST00000682779.1:c.3139+97A= ENSP00000507947.1:n.3139+97A=
ENST00000682845.1:n.2250+97A=
ENST00000682885.1:c.3103+97A= ENSP00000508036.1:n.3103+97A=
ENST00000682933.1:n.3222+97A=
ENST00000683072.1:n.3732+97A=
ENST00000683080.1:n.767+97A=
ENST00000683125.1:c.3256+97A= ENSP00000507939.1:n.3256+97A=
ENST00000683213.1:c.3151+97A= ENSP00000507751.1:n.3151+97A=
ENST00000683220.1:c.3178+97A= ENSP00000507151.1:n.3178+97A=
ENST00000683329.1:n.3951+97A=
ENST00000683346.1:c.*3023+97A= ENSP00000507458.1:n.*3023+97A=
ENST00000683409.1:n.1755+97A=
ENST00000683459.1:n.3735+97A=
ENST00000683590.1:c.2897-5370A= ENSP00000506820.1:n.2897-5370A=
ENST00000683623.1:c.3055+97A= ENSP00000507702.1:n.3055+97A=
ENST00000683645.1:n.3699+97A=
ENST00000683796.1:c.*3020+97A= ENSP00000508221.1:n.*3020+97A=
ENST00000683802.1:n.6073+97A=
ENST00000683833.1:c.3139+97A= ENSP00000506852.1:n.3139+97A=
ENST00000683994.1:c.3148+97A= ENSP00000507181.1:n.3148+97A=
ENST00000684290.1:c.*684+97A= ENSP00000507243.1:n.*684+97A=
ENST00000684306.1:c.*3061+97A= ENSP00000508384.1:n.*3061+97A=
ENST00000684341.1:n.3168+97A=
ENST00000684383.1:c.*2786+97A= ENSP00000506863.1:n.*2786+97A=
ENST00000684619.1:c.*3020+97A= ENSP00000508088.1:n.*3020+97A=
ENST00000684705.1:n.366A=
ENST00000684743.1:n.4179+97A=
ENST00000260665.12:c.3148+97A= MANE Select ENSP00000260665.7:n.3148+97A=
ENST00000260665.11:c.3148+97A= ENSP00000260665.7:n.3148+97A=
NM_133259.3:c.3148+97A= NP_573566.2:n.3148+97A=
XM_006711915.2:c.3070+97A= XP_006711978.1:n.3070+97A=
XM_006711916.2:c.3147+98A= XP_006711979.1:n.3147+98A=
XM_011532473.1:c.3148+97A= XP_011530775.1:n.3148+97A=
XM_011532474.1:c.3148+97A= XP_011530776.1:n.3148+97A=
XM_006711916.3:c.3147+98A= XP_006711979.1:n.3147+98A=
XM_017003117.1:c.3070+97A= XP_016858606.1:n.3070+97A=
XR_002958896.1:n.3190+97A=
NM_133259.4:c.3148+97A= MANE Select NP_573566.2:n.3148+97A=