Canonical Allele Identifier: CA2493975282
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43894633G= , CM000664.2:g.43894633G= GRCh38
NC_000002.11:g.44121772G= , CM000664.1:g.44121772G= GRCh37
NC_000002.10:g.43975276G= NCBI36
NG_008247.1:g.106373C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000419884.6:c.531-4C=
ENST00000681993.1:n.1453-4C=
ENST00000682154.1:n.1335-4C=
ENST00000682303.1:c.*3612-4C= ENSP00000508325.1:n.*3612-4C=
ENST00000682308.1:c.3826-4C= ENSP00000507056.1:n.3826-4C=
ENST00000682434.1:n.3452C=
ENST00000682480.1:c.3919-4C= ENSP00000508344.1:n.3919-4C=
ENST00000682546.1:c.3898-4C= ENSP00000508188.1:n.3898-4C=
ENST00000682585.1:c.*29-4C= ENSP00000506885.1:n.*29-4C=
ENST00000682607.1:c.2644-4C=
ENST00000682612.1:c.752+2001C=
ENST00000682779.1:c.3892-4C= ENSP00000507947.1:n.3892-4C=
ENST00000682885.1:c.3856-4C= ENSP00000508036.1:n.3856-4C=
ENST00000682933.1:n.4101-4C=
ENST00000683002.1:c.753-4C=
ENST00000683072.1:n.4485-4C=
ENST00000683080.1:n.1520-4C=
ENST00000683096.1:n.2342-4C=
ENST00000683125.1:c.4009-4C= ENSP00000507939.1:n.4009-4C=
ENST00000683213.1:c.3904-4C= ENSP00000507751.1:n.3904-4C=
ENST00000683220.1:c.3931-4C= ENSP00000507151.1:n.3931-4C=
ENST00000683329.1:n.4704-4C=
ENST00000683346.1:c.*3776-4C= ENSP00000507458.1:n.*3776-4C=
ENST00000683409.1:n.2433-4C=
ENST00000683459.1:n.4488-4C=
ENST00000683590.1:c.3574-4C= ENSP00000506820.1:n.3574-4C=
ENST00000683623.1:c.3808-4C= ENSP00000507702.1:n.3808-4C=
ENST00000683796.1:c.*3698-4C= ENSP00000508221.1:n.*3698-4C=
ENST00000683833.1:c.3817-4C= ENSP00000506852.1:n.3817-4C=
ENST00000683994.1:c.*14-4C= ENSP00000507181.1:n.*14-4C=
ENST00000684290.1:c.*1362-4C= ENSP00000507243.1:n.*1362-4C=
ENST00000684306.1:c.*3814-4C= ENSP00000508384.1:n.*3814-4C=
ENST00000684383.1:c.*3539-4C= ENSP00000506863.1:n.*3539-4C=
ENST00000684418.1:n.5082-4C=
ENST00000684433.1:n.285-4C=
ENST00000684454.1:n.7761C=
ENST00000684619.1:c.*3773-4C= ENSP00000508088.1:n.*3773-4C=
ENST00000684743.1:n.6646-4C=
ENST00000260665.12:c.3901-4C= MANE Select ENSP00000260665.7:n.3901-4C=
ENST00000260665.11:c.3901-4C= ENSP00000260665.7:n.3901-4C=
ENST00000419884.5:c.142-4C= ENSP00000414207.1:n.142-4C=
ENST00000463456.5:n.2944-4C=
NM_133259.3:c.3901-4C= NP_573566.2:n.3901-4C=
XM_006711915.2:c.3823-4C= XP_006711978.1:n.3823-4C=
XM_011532473.1:c.3826-4C= XP_011530775.1:n.3826-4C=
XM_011532474.1:c.3901-4C= XP_011530776.1:n.3901-4C=
XM_017003117.1:c.3748-4C= XP_016858606.1:n.3748-4C=
XR_002958896.1:n.3943-4C=
NM_133259.4:c.3901-4C= MANE Select NP_573566.2:n.3901-4C=