Canonical Allele Identifier: CA2494001946
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43943843T= , CM000664.2:g.43943843T= GRCh38
NC_000002.11:g.44170982T= , CM000664.1:g.44170982T= GRCh37
NC_000002.10:g.44024486T= NCBI36
NG_008247.1:g.57163A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409659.6:c.2348A= ENSP00000386562.2:p.Asp783=
ENST00000447246.2:c.2348A= ENSP00000403637.2:p.Asp783=
ENST00000681961.1:n.2368A=
ENST00000682104.1:c.2222A= ENSP00000507716.1:p.Asp741=
ENST00000682303.1:c.*2134A= ENSP00000508325.1:n.*2134A=
ENST00000682308.1:c.2348A= ENSP00000507056.1:p.Asp783=
ENST00000682480.1:c.2348A= ENSP00000508344.1:p.Asp783=
ENST00000682546.1:c.2345A= ENSP00000508188.1:p.Asp782=
ENST00000682585.1:c.2348A= ENSP00000506885.1:p.Asp783=
ENST00000682595.1:n.2930A=
ENST00000682607.1:c.766A=
ENST00000682779.1:c.2339A= ENSP00000507947.1:p.Asp780=
ENST00000682845.1:n.1450A=
ENST00000682885.1:c.2303A= ENSP00000508036.1:p.Asp768=
ENST00000682933.1:n.2422A=
ENST00000683072.1:n.2930A=
ENST00000683125.1:c.2348A= ENSP00000507939.1:p.Asp783=
ENST00000683213.1:c.2351A= ENSP00000507751.1:p.Asp784=
ENST00000683220.1:c.2378A= ENSP00000507151.1:p.Asp793=
ENST00000683329.1:n.3151A=
ENST00000683346.1:c.*2223A= ENSP00000507458.1:n.*2223A=
ENST00000683459.1:n.2935A=
ENST00000683590.1:c.2348A= ENSP00000506820.1:p.Asp783=
ENST00000683623.1:c.2297-42A= ENSP00000507702.1:n.2297-42A=
ENST00000683645.1:n.2899A=
ENST00000683694.1:n.1099A=
ENST00000683796.1:c.*2220A= ENSP00000508221.1:n.*2220A=
ENST00000683802.1:n.5273A=
ENST00000683833.1:c.2339A= ENSP00000506852.1:p.Asp780=
ENST00000683989.1:c.2348A= ENSP00000507510.1:p.Asp783=
ENST00000683994.1:c.2348A= ENSP00000507181.1:p.Asp783=
ENST00000684290.1:c.*42A= ENSP00000507243.1:n.*42A=
ENST00000684306.1:c.*2261A= ENSP00000508384.1:n.*2261A=
ENST00000684341.1:n.2368A=
ENST00000684383.1:c.*1986A= ENSP00000506863.1:n.*1986A=
ENST00000684397.1:c.52A=
ENST00000684619.1:c.*2220A= ENSP00000508088.1:n.*2220A=
ENST00000684743.1:n.3379A=
ENST00000260665.12:c.2348A= MANE Select ENSP00000260665.7:p.Asp783=
ENST00000260665.11:c.2348A= ENSP00000260665.7:p.Asp783=
NM_133259.3:c.2348A= NP_573566.2:p.Asp783=
XM_006711915.2:c.2270A= XP_006711978.1:p.Asp757=
XM_006711916.2:c.2348A= XP_006711979.1:p.Asp783=
XM_011532473.1:c.2348A= XP_011530775.1:p.Asp783=
XM_011532474.1:c.2348A= XP_011530776.1:p.Asp783=
XM_006711916.3:c.2348A= XP_006711979.1:p.Asp783=
XM_017003117.1:c.2270A= XP_016858606.1:p.Asp757=
XR_002958896.1:n.2390A=
NM_133259.4:c.2348A= MANE Select NP_573566.2:p.Asp783=