Canonical Allele Identifier: CA2493988077
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43918027T= , CM000664.2:g.43918027T= GRCh38
NC_000002.11:g.44145166T= , CM000664.1:g.44145166T= GRCh37
NC_000002.10:g.43998670T= NCBI36
NG_008247.1:g.82979A=

Transcript Alleles

HGVS Amino-acid change
ENST00000681993.1:n.698A=
ENST00000682295.1:c.303+229A= ENSP00000507499.1:n.303+229A=
ENST00000682303.1:c.*2932A= ENSP00000508325.1:n.*2932A=
ENST00000682308.1:c.3146A= ENSP00000507056.1:p.Lys1049=
ENST00000682480.1:c.3164A= ENSP00000508344.1:p.Lys1055=
ENST00000682546.1:c.3143A= ENSP00000508188.1:p.Lys1048=
ENST00000682585.1:c.3146A= ENSP00000506885.1:p.Lys1049=
ENST00000682595.1:n.3730A=
ENST00000682607.1:c.1564A=
ENST00000682779.1:c.3137A= ENSP00000507947.1:p.Lys1046=
ENST00000682845.1:n.2248A=
ENST00000682885.1:c.3101A= ENSP00000508036.1:p.Lys1034=
ENST00000682933.1:n.3220A=
ENST00000683072.1:n.3730A=
ENST00000683080.1:n.765A=
ENST00000683125.1:c.3254A= ENSP00000507939.1:p.Lys1085=
ENST00000683213.1:c.3149A= ENSP00000507751.1:p.Lys1050=
ENST00000683220.1:c.3176A= ENSP00000507151.1:p.Lys1059=
ENST00000683329.1:n.3949A=
ENST00000683346.1:c.*3021A= ENSP00000507458.1:n.*3021A=
ENST00000683409.1:n.1753A=
ENST00000683459.1:n.3733A=
ENST00000683590.1:c.2897-5469A= ENSP00000506820.1:n.2897-5469A=
ENST00000683623.1:c.3053A= ENSP00000507702.1:p.Lys1018=
ENST00000683645.1:n.3697A=
ENST00000683796.1:c.*3018A= ENSP00000508221.1:n.*3018A=
ENST00000683802.1:n.6071A=
ENST00000683833.1:c.3137A= ENSP00000506852.1:p.Lys1046=
ENST00000683994.1:c.3146A= ENSP00000507181.1:p.Lys1049=
ENST00000684290.1:c.*682A= ENSP00000507243.1:n.*682A=
ENST00000684306.1:c.*3059A= ENSP00000508384.1:n.*3059A=
ENST00000684341.1:n.3166A=
ENST00000684383.1:c.*2784A= ENSP00000506863.1:n.*2784A=
ENST00000684619.1:c.*3018A= ENSP00000508088.1:n.*3018A=
ENST00000684705.1:n.267A=
ENST00000684743.1:n.4177A=
ENST00000260665.12:c.3146A= MANE Select ENSP00000260665.7:p.Lys1049=
ENST00000260665.11:c.3146A= ENSP00000260665.7:p.Lys1049=
NM_133259.3:c.3146A= NP_573566.2:p.Lys1049=
XM_006711915.2:c.3068A= XP_006711978.1:p.Lys1023=
XM_006711916.2:c.3146A= XP_006711979.1:p.Lys1049=
XM_011532473.1:c.3146A= XP_011530775.1:p.Lys1049=
XM_011532474.1:c.3146A= XP_011530776.1:p.Lys1049=
XM_006711916.3:c.3146A= XP_006711979.1:p.Lys1049=
XM_017003117.1:c.3068A= XP_016858606.1:p.Lys1023=
XR_002958896.1:n.3188A=
NM_133259.4:c.3146A= MANE Select NP_573566.2:p.Lys1049=