Canonical Allele Identifier: CA2493988092
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43918045C= , CM000664.2:g.43918045C= GRCh38
NC_000002.11:g.44145184C= , CM000664.1:g.44145184C= GRCh37
NC_000002.10:g.43998688C= NCBI36
NG_008247.1:g.82961G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000681993.1:n.680G=
ENST00000682295.1:c.303+211G= ENSP00000507499.1:n.303+211G=
ENST00000682303.1:c.*2914G= ENSP00000508325.1:n.*2914G=
ENST00000682308.1:c.3128G= ENSP00000507056.1:p.Cys1043=
ENST00000682480.1:c.3146G= ENSP00000508344.1:p.Cys1049=
ENST00000682546.1:c.3125G= ENSP00000508188.1:p.Cys1042=
ENST00000682585.1:c.3128G= ENSP00000506885.1:p.Cys1043=
ENST00000682595.1:n.3712G=
ENST00000682607.1:c.1546G=
ENST00000682779.1:c.3119G= ENSP00000507947.1:p.Cys1040=
ENST00000682845.1:n.2230G=
ENST00000682885.1:c.3083G= ENSP00000508036.1:p.Cys1028=
ENST00000682933.1:n.3202G=
ENST00000683072.1:n.3712G=
ENST00000683080.1:n.747G=
ENST00000683125.1:c.3236G= ENSP00000507939.1:p.Cys1079=
ENST00000683213.1:c.3131G= ENSP00000507751.1:p.Cys1044=
ENST00000683220.1:c.3158G= ENSP00000507151.1:p.Cys1053=
ENST00000683329.1:n.3931G=
ENST00000683346.1:c.*3003G= ENSP00000507458.1:n.*3003G=
ENST00000683409.1:n.1735G=
ENST00000683459.1:n.3715G=
ENST00000683590.1:c.2897-5487G= ENSP00000506820.1:n.2897-5487G=
ENST00000683623.1:c.3035G= ENSP00000507702.1:p.Cys1012=
ENST00000683645.1:n.3679G=
ENST00000683796.1:c.*3000G= ENSP00000508221.1:n.*3000G=
ENST00000683802.1:n.6053G=
ENST00000683833.1:c.3119G= ENSP00000506852.1:p.Cys1040=
ENST00000683994.1:c.3128G= ENSP00000507181.1:p.Cys1043=
ENST00000684290.1:c.*664G= ENSP00000507243.1:n.*664G=
ENST00000684306.1:c.*3041G= ENSP00000508384.1:n.*3041G=
ENST00000684341.1:n.3148G=
ENST00000684383.1:c.*2766G= ENSP00000506863.1:n.*2766G=
ENST00000684619.1:c.*3000G= ENSP00000508088.1:n.*3000G=
ENST00000684705.1:n.249G=
ENST00000684743.1:n.4159G=
ENST00000260665.12:c.3128G= MANE Select ENSP00000260665.7:p.Cys1043=
ENST00000260665.11:c.3128G= ENSP00000260665.7:p.Cys1043=
NM_133259.3:c.3128G= NP_573566.2:p.Cys1043=
XM_006711915.2:c.3050G= XP_006711978.1:p.Cys1017=
XM_006711916.2:c.3128G= XP_006711979.1:p.Cys1043=
XM_011532473.1:c.3128G= XP_011530775.1:p.Cys1043=
XM_011532474.1:c.3128G= XP_011530776.1:p.Cys1043=
XM_006711916.3:c.3128G= XP_006711979.1:p.Cys1043=
XM_017003117.1:c.3050G= XP_016858606.1:p.Cys1017=
XR_002958896.1:n.3170G=
NM_133259.4:c.3128G= MANE Select NP_573566.2:p.Cys1043=