Canonical Allele Identifier: CA2494004297
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43948179A= , CM000664.2:g.43948179A= GRCh38
NC_000002.11:g.44175318A= , CM000664.1:g.44175318A= GRCh37
NC_000002.10:g.44028822A= NCBI36
NG_008247.1:g.52827T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409659.6:c.1863T= ENSP00000386562.2:p.Asn621=
ENST00000447246.2:c.1863T= ENSP00000403637.2:p.Asn621=
ENST00000467058.2:n.592T=
ENST00000681959.1:n.1477T=
ENST00000681961.1:n.1883T=
ENST00000682104.1:c.1737T= ENSP00000507716.1:p.Asn579=
ENST00000682303.1:c.*1735T= ENSP00000508325.1:n.*1735T=
ENST00000682308.1:c.1863T= ENSP00000507056.1:p.Asn621=
ENST00000682480.1:c.1863T= ENSP00000508344.1:p.Asn621=
ENST00000682546.1:c.1860T= ENSP00000508188.1:p.Asn620=
ENST00000682585.1:c.1863T= ENSP00000506885.1:p.Asn621=
ENST00000682595.1:n.2445T=
ENST00000682607.1:c.281T=
ENST00000682779.1:c.1854T= ENSP00000507947.1:p.Asn618=
ENST00000682885.1:c.1863T= ENSP00000508036.1:p.Asn621=
ENST00000682933.1:n.1937T=
ENST00000683072.1:n.2445T=
ENST00000683082.1:n.1881T=
ENST00000683125.1:c.1863T= ENSP00000507939.1:p.Asn621=
ENST00000683213.1:c.1866T= ENSP00000507751.1:p.Asn622=
ENST00000683220.1:c.1893T= ENSP00000507151.1:p.Asn631=
ENST00000683329.1:n.2666T=
ENST00000683346.1:c.*1738T= ENSP00000507458.1:n.*1738T=
ENST00000683459.1:n.2450T=
ENST00000683590.1:c.1863T= ENSP00000506820.1:p.Asn621=
ENST00000683623.1:c.1863T= ENSP00000507702.1:p.Asn621=
ENST00000683645.1:n.2414T=
ENST00000683694.1:n.614T=
ENST00000683796.1:c.*1735T= ENSP00000508221.1:n.*1735T=
ENST00000683802.1:n.4788T=
ENST00000683833.1:c.1854T= ENSP00000506852.1:p.Asn618=
ENST00000683934.1:c.1749T=
ENST00000683989.1:c.1863T= ENSP00000507510.1:p.Asn621=
ENST00000683994.1:c.1863T= ENSP00000507181.1:p.Asn621=
ENST00000684290.1:c.1863T= ENSP00000507243.1:p.Asn621=
ENST00000684306.1:c.*1776T= ENSP00000508384.1:n.*1776T=
ENST00000684341.1:n.1883T=
ENST00000684383.1:c.*1501T= ENSP00000506863.1:n.*1501T=
ENST00000684482.1:c.4332T=
ENST00000684619.1:c.*1735T= ENSP00000508088.1:n.*1735T=
ENST00000684743.1:n.2894T=
ENST00000260665.12:c.1863T= MANE Select ENSP00000260665.7:p.Asn621=
ENST00000260665.11:c.1863T= ENSP00000260665.7:p.Asn621=
NM_133259.3:c.1863T= NP_573566.2:p.Asn621=
XM_006711915.2:c.1785T= XP_006711978.1:p.Asn595=
XM_006711916.2:c.1863T= XP_006711979.1:p.Asn621=
XM_011532473.1:c.1863T= XP_011530775.1:p.Asn621=
XM_011532474.1:c.1863T= XP_011530776.1:p.Asn621=
XM_006711916.3:c.1863T= XP_006711979.1:p.Asn621=
XM_017003117.1:c.1785T= XP_016858606.1:p.Asn595=
XR_002958896.1:n.1905T=
NM_133259.4:c.1863T= MANE Select NP_573566.2:p.Asn621=