Canonical Allele Identifier: CA2493981267
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43905766A= , CM000664.2:g.43905766A= GRCh38
NC_000002.11:g.44132905A= , CM000664.1:g.44132905A= GRCh37
NC_000002.10:g.43986409A= NCBI36
NG_008247.1:g.95240T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000472420.6:n.369T=
ENST00000681993.1:n.842T=
ENST00000682295.1:c.445T= ENSP00000507499.1:n.445T=
ENST00000682303.1:c.*3076T= ENSP00000508325.1:n.*3076T=
ENST00000682308.1:c.3290T= ENSP00000507056.1:p.Ile1097=
ENST00000682480.1:c.3308T= ENSP00000508344.1:p.Ile1103=
ENST00000682546.1:c.3287T= ENSP00000508188.1:p.Ile1096=
ENST00000682585.1:c.3290T= ENSP00000506885.1:p.Ile1097=
ENST00000682595.1:n.3874T=
ENST00000682607.1:c.1708T=
ENST00000682612.1:c.142T=
ENST00000682779.1:c.3281T= ENSP00000507947.1:p.Ile1094=
ENST00000682845.1:n.2392T=
ENST00000682885.1:c.3245T= ENSP00000508036.1:p.Ile1082=
ENST00000682933.1:n.3364T=
ENST00000683002.1:c.142T=
ENST00000683072.1:n.3874T=
ENST00000683080.1:n.909T=
ENST00000683125.1:c.3398T= ENSP00000507939.1:p.Ile1133=
ENST00000683213.1:c.3293T= ENSP00000507751.1:p.Ile1098=
ENST00000683220.1:c.3320T= ENSP00000507151.1:p.Ile1107=
ENST00000683329.1:n.4093T=
ENST00000683346.1:c.*3165T= ENSP00000507458.1:n.*3165T=
ENST00000683409.1:n.1897T=
ENST00000683459.1:n.3877T=
ENST00000683528.1:c.142T=
ENST00000683590.1:c.3038T= ENSP00000506820.1:p.Ile1013=
ENST00000683623.1:c.3197T= ENSP00000507702.1:p.Ile1066=
ENST00000683645.1:n.3841T=
ENST00000683796.1:c.*3162T= ENSP00000508221.1:n.*3162T=
ENST00000683802.1:n.6215T=
ENST00000683833.1:c.3281T= ENSP00000506852.1:p.Ile1094=
ENST00000683994.1:c.3290T= ENSP00000507181.1:p.Ile1097=
ENST00000684290.1:c.*826T= ENSP00000507243.1:n.*826T=
ENST00000684306.1:c.*3203T= ENSP00000508384.1:n.*3203T=
ENST00000684341.1:n.3310T=
ENST00000684383.1:c.*2928T= ENSP00000506863.1:n.*2928T=
ENST00000684418.1:n.4471T=
ENST00000684454.1:n.2640T=
ENST00000684619.1:c.*3162T= ENSP00000508088.1:n.*3162T=
ENST00000684743.1:n.4321T=
ENST00000260665.12:c.3290T= MANE Select ENSP00000260665.7:p.Ile1097=
ENST00000260665.11:c.3290T= ENSP00000260665.7:p.Ile1097=
NM_133259.3:c.3290T= NP_573566.2:p.Ile1097=
XM_006711915.2:c.3212T= XP_006711978.1:p.Ile1071=
XM_011532473.1:c.3290T= XP_011530775.1:p.Ile1097=
XM_011532474.1:c.3290T= XP_011530776.1:p.Ile1097=
XM_017003117.1:c.3212T= XP_016858606.1:p.Ile1071=
XR_002958896.1:n.3332T=
NM_133259.4:c.3290T= MANE Select NP_573566.2:p.Ile1097=