Canonical Allele Identifier: CA2493988108
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43918085T= , CM000664.2:g.43918085T= GRCh38
NC_000002.11:g.44145224T= , CM000664.1:g.44145224T= GRCh37
NC_000002.10:g.43998728T= NCBI36
NG_008247.1:g.82921A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000681993.1:n.640A=
ENST00000682295.1:c.303+171A= ENSP00000507499.1:n.303+171A=
ENST00000682303.1:c.*2874A= ENSP00000508325.1:n.*2874A=
ENST00000682308.1:c.3088A= ENSP00000507056.1:p.Thr1030=
ENST00000682480.1:c.3106A= ENSP00000508344.1:p.Thr1036=
ENST00000682546.1:c.3085A= ENSP00000508188.1:p.Thr1029=
ENST00000682585.1:c.3088A= ENSP00000506885.1:p.Thr1030=
ENST00000682595.1:n.3672A=
ENST00000682607.1:c.1506A=
ENST00000682779.1:c.3079A= ENSP00000507947.1:p.Thr1027=
ENST00000682845.1:n.2190A=
ENST00000682885.1:c.3043A= ENSP00000508036.1:p.Thr1015=
ENST00000682933.1:n.3162A=
ENST00000683072.1:n.3672A=
ENST00000683080.1:n.707A=
ENST00000683125.1:c.3196A= ENSP00000507939.1:p.Thr1066=
ENST00000683213.1:c.3091A= ENSP00000507751.1:p.Thr1031=
ENST00000683220.1:c.3118A= ENSP00000507151.1:p.Thr1040=
ENST00000683329.1:n.3891A=
ENST00000683346.1:c.*2963A= ENSP00000507458.1:n.*2963A=
ENST00000683409.1:n.1695A=
ENST00000683459.1:n.3675A=
ENST00000683590.1:c.2897-5527A= ENSP00000506820.1:n.2897-5527A=
ENST00000683623.1:c.2995A= ENSP00000507702.1:p.Thr999=
ENST00000683645.1:n.3639A=
ENST00000683796.1:c.*2960A= ENSP00000508221.1:n.*2960A=
ENST00000683802.1:n.6013A=
ENST00000683833.1:c.3079A= ENSP00000506852.1:p.Thr1027=
ENST00000683994.1:c.3088A= ENSP00000507181.1:p.Thr1030=
ENST00000684290.1:c.*624A= ENSP00000507243.1:n.*624A=
ENST00000684306.1:c.*3001A= ENSP00000508384.1:n.*3001A=
ENST00000684341.1:n.3108A=
ENST00000684383.1:c.*2726A= ENSP00000506863.1:n.*2726A=
ENST00000684619.1:c.*2960A= ENSP00000508088.1:n.*2960A=
ENST00000684705.1:n.209A=
ENST00000684743.1:n.4119A=
ENST00000260665.12:c.3088A= MANE Select ENSP00000260665.7:p.Thr1030=
ENST00000260665.11:c.3088A= ENSP00000260665.7:p.Thr1030=
NM_133259.3:c.3088A= NP_573566.2:p.Thr1030=
XM_006711915.2:c.3010A= XP_006711978.1:p.Thr1004=
XM_006711916.2:c.3088A= XP_006711979.1:p.Thr1030=
XM_011532473.1:c.3088A= XP_011530775.1:p.Thr1030=
XM_011532474.1:c.3088A= XP_011530776.1:p.Thr1030=
XM_006711916.3:c.3088A= XP_006711979.1:p.Thr1030=
XM_017003117.1:c.3010A= XP_016858606.1:p.Thr1004=
XR_002958896.1:n.3130A=
NM_133259.4:c.3088A= MANE Select NP_573566.2:p.Thr1030=