Canonical Allele Identifier: CA2493988235
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43918358A= , CM000664.2:g.43918358A= GRCh38
NC_000002.11:g.44145497A= , CM000664.1:g.44145497A= GRCh37
NC_000002.10:g.43999001A= NCBI36
NG_008247.1:g.82648T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000681993.1:n.489T=
ENST00000682295.1:c.201T= ENSP00000507499.1:p.Asn67=
ENST00000682303.1:c.*2723T= ENSP00000508325.1:n.*2723T=
ENST00000682308.1:c.2937T= ENSP00000507056.1:p.Asn979=
ENST00000682480.1:c.2937T= ENSP00000508344.1:p.Asn979=
ENST00000682546.1:c.2934T= ENSP00000508188.1:p.Asn978=
ENST00000682585.1:c.2937T= ENSP00000506885.1:p.Asn979=
ENST00000682595.1:n.3521T=
ENST00000682607.1:c.1355T=
ENST00000682779.1:c.2928T= ENSP00000507947.1:p.Asn976=
ENST00000682845.1:n.2039T=
ENST00000682885.1:c.2892T= ENSP00000508036.1:p.Asn964=
ENST00000682933.1:n.3011T=
ENST00000683072.1:n.3521T=
ENST00000683080.1:n.556T=
ENST00000683125.1:c.3045T= ENSP00000507939.1:p.Asn1015=
ENST00000683213.1:c.2940T= ENSP00000507751.1:p.Asn980=
ENST00000683220.1:c.2967T= ENSP00000507151.1:p.Asn989=
ENST00000683236.1:c.267T= ENSP00000506891.1:n.267T=
ENST00000683329.1:n.3740T=
ENST00000683346.1:c.*2812T= ENSP00000507458.1:n.*2812T=
ENST00000683409.1:n.1544T=
ENST00000683459.1:n.3524T=
ENST00000683590.1:c.2897-5800T= ENSP00000506820.1:n.2897-5800T=
ENST00000683623.1:c.2844T= ENSP00000507702.1:p.Asn948=
ENST00000683645.1:n.3488T=
ENST00000683796.1:c.*2809T= ENSP00000508221.1:n.*2809T=
ENST00000683802.1:n.5862T=
ENST00000683833.1:c.2928T= ENSP00000506852.1:p.Asn976=
ENST00000683994.1:c.2937T= ENSP00000507181.1:p.Asn979=
ENST00000684290.1:c.*473T= ENSP00000507243.1:n.*473T=
ENST00000684306.1:c.*2850T= ENSP00000508384.1:n.*2850T=
ENST00000684341.1:n.2957T=
ENST00000684383.1:c.*2575T= ENSP00000506863.1:n.*2575T=
ENST00000684619.1:c.*2809T= ENSP00000508088.1:n.*2809T=
ENST00000684705.1:n.58T=
ENST00000684743.1:n.3968T=
ENST00000260665.12:c.2937T= MANE Select ENSP00000260665.7:p.Asn979=
ENST00000260665.11:c.2937T= ENSP00000260665.7:p.Asn979=
NM_133259.3:c.2937T= NP_573566.2:p.Asn979=
XM_006711915.2:c.2859T= XP_006711978.1:p.Asn953=
XM_006711916.2:c.2937T= XP_006711979.1:p.Asn979=
XM_011532473.1:c.2937T= XP_011530775.1:p.Asn979=
XM_011532474.1:c.2937T= XP_011530776.1:p.Asn979=
XM_006711916.3:c.2937T= XP_006711979.1:p.Asn979=
XM_017003117.1:c.2859T= XP_016858606.1:p.Asn953=
XR_002958896.1:n.2979T=
NM_133259.4:c.2937T= MANE Select NP_573566.2:p.Asn979=