Canonical Allele Identifier: CA2493988086
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43918039A= , CM000664.2:g.43918039A= GRCh38
NC_000002.11:g.44145178A= , CM000664.1:g.44145178A= GRCh37
NC_000002.10:g.43998682A= NCBI36
NG_008247.1:g.82967T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000681993.1:n.686T=
ENST00000682295.1:c.303+217T= ENSP00000507499.1:n.303+217T=
ENST00000682303.1:c.*2920T= ENSP00000508325.1:n.*2920T=
ENST00000682308.1:c.3134T= ENSP00000507056.1:p.Leu1045=
ENST00000682480.1:c.3152T= ENSP00000508344.1:p.Leu1051=
ENST00000682546.1:c.3131T= ENSP00000508188.1:p.Leu1044=
ENST00000682585.1:c.3134T= ENSP00000506885.1:p.Leu1045=
ENST00000682595.1:n.3718T=
ENST00000682607.1:c.1552T=
ENST00000682779.1:c.3125T= ENSP00000507947.1:p.Leu1042=
ENST00000682845.1:n.2236T=
ENST00000682885.1:c.3089T= ENSP00000508036.1:p.Leu1030=
ENST00000682933.1:n.3208T=
ENST00000683072.1:n.3718T=
ENST00000683080.1:n.753T=
ENST00000683125.1:c.3242T= ENSP00000507939.1:p.Leu1081=
ENST00000683213.1:c.3137T= ENSP00000507751.1:p.Leu1046=
ENST00000683220.1:c.3164T= ENSP00000507151.1:p.Leu1055=
ENST00000683329.1:n.3937T=
ENST00000683346.1:c.*3009T= ENSP00000507458.1:n.*3009T=
ENST00000683409.1:n.1741T=
ENST00000683459.1:n.3721T=
ENST00000683590.1:c.2897-5481T= ENSP00000506820.1:n.2897-5481T=
ENST00000683623.1:c.3041T= ENSP00000507702.1:p.Leu1014=
ENST00000683645.1:n.3685T=
ENST00000683796.1:c.*3006T= ENSP00000508221.1:n.*3006T=
ENST00000683802.1:n.6059T=
ENST00000683833.1:c.3125T= ENSP00000506852.1:p.Leu1042=
ENST00000683994.1:c.3134T= ENSP00000507181.1:p.Leu1045=
ENST00000684290.1:c.*670T= ENSP00000507243.1:n.*670T=
ENST00000684306.1:c.*3047T= ENSP00000508384.1:n.*3047T=
ENST00000684341.1:n.3154T=
ENST00000684383.1:c.*2772T= ENSP00000506863.1:n.*2772T=
ENST00000684619.1:c.*3006T= ENSP00000508088.1:n.*3006T=
ENST00000684705.1:n.255T=
ENST00000684743.1:n.4165T=
ENST00000260665.12:c.3134T= MANE Select ENSP00000260665.7:p.Leu1045=
ENST00000260665.11:c.3134T= ENSP00000260665.7:p.Leu1045=
NM_133259.3:c.3134T= NP_573566.2:p.Leu1045=
XM_006711915.2:c.3056T= XP_006711978.1:p.Leu1019=
XM_006711916.2:c.3134T= XP_006711979.1:p.Leu1045=
XM_011532473.1:c.3134T= XP_011530775.1:p.Leu1045=
XM_011532474.1:c.3134T= XP_011530776.1:p.Leu1045=
XM_006711916.3:c.3134T= XP_006711979.1:p.Leu1045=
XM_017003117.1:c.3056T= XP_016858606.1:p.Leu1019=
XR_002958896.1:n.3176T=
NM_133259.4:c.3134T= MANE Select NP_573566.2:p.Leu1045=