Canonical Allele Identifier: CA2494020602
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43977159T= , CM000664.2:g.43977159T= GRCh38
NC_000002.11:g.44204298T= , CM000664.1:g.44204298T= GRCh37
NC_000002.10:g.44057802T= NCBI36
NG_008247.1:g.23847A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409659.6:c.587A= ENSP00000386562.2:p.Asn196=
ENST00000409946.6:c.587A= ENSP00000386234.1:p.Asn196=
ENST00000447246.2:c.587A= ENSP00000403637.2:p.Asn196=
ENST00000681959.1:n.201A=
ENST00000681961.1:n.607A=
ENST00000682104.1:c.461A= ENSP00000507716.1:p.Asn154=
ENST00000682303.1:c.*459A= ENSP00000508325.1:n.*459A=
ENST00000682308.1:c.587A= ENSP00000507056.1:p.Asn196=
ENST00000682480.1:c.587A= ENSP00000508344.1:p.Asn196=
ENST00000682496.1:n.551A=
ENST00000682546.1:c.587A= ENSP00000508188.1:p.Asn196=
ENST00000682585.1:c.587A= ENSP00000506885.1:p.Asn196=
ENST00000682595.1:n.602A=
ENST00000682779.1:c.578A= ENSP00000507947.1:p.Asn193=
ENST00000682885.1:c.587A= ENSP00000508036.1:p.Asn196=
ENST00000683072.1:n.602A=
ENST00000683082.1:n.605A=
ENST00000683125.1:c.587A= ENSP00000507939.1:p.Asn196=
ENST00000683213.1:c.587A= ENSP00000507751.1:p.Asn196=
ENST00000683220.1:c.587A= ENSP00000507151.1:p.Asn196=
ENST00000683329.1:n.626A=
ENST00000683346.1:c.*459A= ENSP00000507458.1:n.*459A=
ENST00000683459.1:n.607A=
ENST00000683590.1:c.587A= ENSP00000506820.1:p.Asn196=
ENST00000683623.1:c.587A= ENSP00000507702.1:p.Asn196=
ENST00000683796.1:c.*459A= ENSP00000508221.1:n.*459A=
ENST00000683802.1:n.423A=
ENST00000683833.1:c.578A= ENSP00000506852.1:p.Asn193=
ENST00000683934.1:c.241A=
ENST00000683989.1:c.587A= ENSP00000507510.1:p.Asn196=
ENST00000683994.1:c.587A= ENSP00000507181.1:p.Asn196=
ENST00000684290.1:c.587A= ENSP00000507243.1:p.Asn196=
ENST00000684306.1:c.*500A= ENSP00000508384.1:n.*500A=
ENST00000684329.1:n.629A=
ENST00000684341.1:n.607A=
ENST00000684383.1:c.*225A= ENSP00000506863.1:n.*225A=
ENST00000684482.1:c.241A=
ENST00000684619.1:c.*459A= ENSP00000508088.1:n.*459A=
ENST00000684691.1:n.629A=
ENST00000260665.12:c.587A= MANE Select ENSP00000260665.7:p.Asn196=
ENST00000260665.11:c.587A= ENSP00000260665.7:p.Asn196=
ENST00000409659.5:c.587A= ENSP00000386562.1:p.Asn196=
ENST00000409946.5:c.587A= ENSP00000386234.1:p.Asn196=
ENST00000447246.1:c.509A= ENSP00000403637.1:p.Asn170=
NM_133259.3:c.587A= NP_573566.2:p.Asn196=
XM_006711915.2:c.509A= XP_006711978.1:p.Asn170=
XM_006711916.2:c.587A= XP_006711979.1:p.Asn196=
XM_011532473.1:c.587A= XP_011530775.1:p.Asn196=
XM_011532474.1:c.587A= XP_011530776.1:p.Asn196=
XM_006711916.3:c.587A= XP_006711979.1:p.Asn196=
XM_017003117.1:c.509A= XP_016858606.1:p.Asn170=
XR_002958896.1:n.629A=
NM_133259.4:c.587A= MANE Select NP_573566.2:p.Asn196=