Canonical Allele Identifier: CA2493988239
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43918368G= , CM000664.2:g.43918368G= GRCh38
NC_000002.11:g.44145507G= , CM000664.1:g.44145507G= GRCh37
NC_000002.10:g.43999011G= NCBI36
NG_008247.1:g.82638C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000681993.1:n.479C=
ENST00000682295.1:c.191C= ENSP00000507499.1:p.Ala64=
ENST00000682303.1:c.*2713C= ENSP00000508325.1:n.*2713C=
ENST00000682308.1:c.2927C= ENSP00000507056.1:p.Ala976=
ENST00000682480.1:c.2927C= ENSP00000508344.1:p.Ala976=
ENST00000682546.1:c.2924C= ENSP00000508188.1:p.Ala975=
ENST00000682585.1:c.2927C= ENSP00000506885.1:p.Ala976=
ENST00000682595.1:n.3511C=
ENST00000682607.1:c.1345C=
ENST00000682779.1:c.2918C= ENSP00000507947.1:p.Ala973=
ENST00000682845.1:n.2029C=
ENST00000682885.1:c.2882C= ENSP00000508036.1:p.Ala961=
ENST00000682933.1:n.3001C=
ENST00000683072.1:n.3511C=
ENST00000683080.1:n.546C=
ENST00000683125.1:c.3035C= ENSP00000507939.1:p.Ala1012=
ENST00000683213.1:c.2930C= ENSP00000507751.1:p.Ala977=
ENST00000683220.1:c.2957C= ENSP00000507151.1:p.Ala986=
ENST00000683236.1:c.257C= ENSP00000506891.1:n.257C=
ENST00000683329.1:n.3730C=
ENST00000683346.1:c.*2802C= ENSP00000507458.1:n.*2802C=
ENST00000683409.1:n.1534C=
ENST00000683459.1:n.3514C=
ENST00000683590.1:c.2897-5810C= ENSP00000506820.1:n.2897-5810C=
ENST00000683623.1:c.2834C= ENSP00000507702.1:p.Ala945=
ENST00000683645.1:n.3478C=
ENST00000683796.1:c.*2799C= ENSP00000508221.1:n.*2799C=
ENST00000683802.1:n.5852C=
ENST00000683833.1:c.2918C= ENSP00000506852.1:p.Ala973=
ENST00000683994.1:c.2927C= ENSP00000507181.1:p.Ala976=
ENST00000684290.1:c.*463C= ENSP00000507243.1:n.*463C=
ENST00000684306.1:c.*2840C= ENSP00000508384.1:n.*2840C=
ENST00000684341.1:n.2947C=
ENST00000684383.1:c.*2565C= ENSP00000506863.1:n.*2565C=
ENST00000684619.1:c.*2799C= ENSP00000508088.1:n.*2799C=
ENST00000684705.1:n.48C=
ENST00000684743.1:n.3958C=
ENST00000260665.12:c.2927C= MANE Select ENSP00000260665.7:p.Ala976=
ENST00000260665.11:c.2927C= ENSP00000260665.7:p.Ala976=
NM_133259.3:c.2927C= NP_573566.2:p.Ala976=
XM_006711915.2:c.2849C= XP_006711978.1:p.Ala950=
XM_006711916.2:c.2927C= XP_006711979.1:p.Ala976=
XM_011532473.1:c.2927C= XP_011530775.1:p.Ala976=
XM_011532474.1:c.2927C= XP_011530776.1:p.Ala976=
XM_006711916.3:c.2927C= XP_006711979.1:p.Ala976=
XM_017003117.1:c.2849C= XP_016858606.1:p.Ala950=
XR_002958896.1:n.2969C=
NM_133259.4:c.2927C= MANE Select NP_573566.2:p.Ala976=