Canonical Allele Identifier: CA2493988106
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43918083G= , CM000664.2:g.43918083G= GRCh38
NC_000002.11:g.44145222G= , CM000664.1:g.44145222G= GRCh37
NC_000002.10:g.43998726G= NCBI36
NG_008247.1:g.82923C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000681993.1:n.642C=
ENST00000682295.1:c.303+173C= ENSP00000507499.1:n.303+173C=
ENST00000682303.1:c.*2876C= ENSP00000508325.1:n.*2876C=
ENST00000682308.1:c.3090C= ENSP00000507056.1:p.Thr1030=
ENST00000682480.1:c.3108C= ENSP00000508344.1:p.Thr1036=
ENST00000682546.1:c.3087C= ENSP00000508188.1:p.Thr1029=
ENST00000682585.1:c.3090C= ENSP00000506885.1:p.Thr1030=
ENST00000682595.1:n.3674C=
ENST00000682607.1:c.1508C=
ENST00000682779.1:c.3081C= ENSP00000507947.1:p.Thr1027=
ENST00000682845.1:n.2192C=
ENST00000682885.1:c.3045C= ENSP00000508036.1:p.Thr1015=
ENST00000682933.1:n.3164C=
ENST00000683072.1:n.3674C=
ENST00000683080.1:n.709C=
ENST00000683125.1:c.3198C= ENSP00000507939.1:p.Thr1066=
ENST00000683213.1:c.3093C= ENSP00000507751.1:p.Thr1031=
ENST00000683220.1:c.3120C= ENSP00000507151.1:p.Thr1040=
ENST00000683329.1:n.3893C=
ENST00000683346.1:c.*2965C= ENSP00000507458.1:n.*2965C=
ENST00000683409.1:n.1697C=
ENST00000683459.1:n.3677C=
ENST00000683590.1:c.2897-5525C= ENSP00000506820.1:n.2897-5525C=
ENST00000683623.1:c.2997C= ENSP00000507702.1:p.Thr999=
ENST00000683645.1:n.3641C=
ENST00000683796.1:c.*2962C= ENSP00000508221.1:n.*2962C=
ENST00000683802.1:n.6015C=
ENST00000683833.1:c.3081C= ENSP00000506852.1:p.Thr1027=
ENST00000683994.1:c.3090C= ENSP00000507181.1:p.Thr1030=
ENST00000684290.1:c.*626C= ENSP00000507243.1:n.*626C=
ENST00000684306.1:c.*3003C= ENSP00000508384.1:n.*3003C=
ENST00000684341.1:n.3110C=
ENST00000684383.1:c.*2728C= ENSP00000506863.1:n.*2728C=
ENST00000684619.1:c.*2962C= ENSP00000508088.1:n.*2962C=
ENST00000684705.1:n.211C=
ENST00000684743.1:n.4121C=
ENST00000260665.12:c.3090C= MANE Select ENSP00000260665.7:p.Thr1030=
ENST00000260665.11:c.3090C= ENSP00000260665.7:p.Thr1030=
NM_133259.3:c.3090C= NP_573566.2:p.Thr1030=
XM_006711915.2:c.3012C= XP_006711978.1:p.Thr1004=
XM_006711916.2:c.3090C= XP_006711979.1:p.Thr1030=
XM_011532473.1:c.3090C= XP_011530775.1:p.Thr1030=
XM_011532474.1:c.3090C= XP_011530776.1:p.Thr1030=
XM_006711916.3:c.3090C= XP_006711979.1:p.Thr1030=
XM_017003117.1:c.3012C= XP_016858606.1:p.Thr1004=
XR_002958896.1:n.3132C=
NM_133259.4:c.3090C= MANE Select NP_573566.2:p.Thr1030=