Canonical Allele Identifier: CA346678567
Gene: LRPPRC HGNC NCBI

Linked Data

dbSNP Id: rs368696980
gnomAD v4: 2-43957433-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43957433G>A , CM000664.2:g.43957433G>A GRCh38
NC_000002.11:g.44184572G>A , CM000664.1:g.44184572G>A GRCh37
NC_000002.10:g.44038076G>A NCBI36
NG_008247.1:g.43573C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000409659.6:c.1601C>T ENSP00000386562.2:p.Pro534Leu
ENST00000447246.2:c.1601C>T ENSP00000403637.2:p.Pro534Leu
ENST00000467058.2:n.330C>T
ENST00000681959.1:n.1215C>T
ENST00000681961.1:n.1621C>T
ENST00000682104.1:c.1475C>T ENSP00000507716.1:p.Pro492Leu
ENST00000682303.1:c.*1473C>T ENSP00000508325.1:n.*1473C>T
ENST00000682308.1:c.1601C>T ENSP00000507056.1:p.Pro534Leu
ENST00000682480.1:c.1601C>T ENSP00000508344.1:p.Pro534Leu
ENST00000682546.1:c.1601C>T ENSP00000508188.1:p.Pro534Leu
ENST00000682585.1:c.1601C>T ENSP00000506885.1:p.Pro534Leu
ENST00000682595.1:n.2183C>T
ENST00000682607.1:c.19C>T
ENST00000682779.1:c.1592C>T ENSP00000507947.1:p.Pro531Leu
ENST00000682885.1:c.1601C>T ENSP00000508036.1:p.Pro534Leu
ENST00000682933.1:n.1675C>T
ENST00000683072.1:n.2183C>T
ENST00000683082.1:n.1619C>T
ENST00000683125.1:c.1601C>T ENSP00000507939.1:p.Pro534Leu
ENST00000683213.1:c.1604C>T ENSP00000507751.1:p.Pro535Leu
ENST00000683220.1:c.1601C>T ENSP00000507151.1:p.Pro534Leu
ENST00000683329.1:n.2404C>T
ENST00000683346.1:c.*1476C>T ENSP00000507458.1:n.*1476C>T
ENST00000683459.1:n.2188C>T
ENST00000683590.1:c.1601C>T ENSP00000506820.1:p.Pro534Leu
ENST00000683623.1:c.1601C>T ENSP00000507702.1:p.Pro534Leu
ENST00000683645.1:n.2121C>T
ENST00000683694.1:n.352C>T
ENST00000683796.1:c.*1473C>T ENSP00000508221.1:n.*1473C>T
ENST00000683802.1:n.4526C>T
ENST00000683833.1:c.1592C>T ENSP00000506852.1:p.Pro531Leu
ENST00000683934.1:c.1487C>T
ENST00000683989.1:c.1601C>T ENSP00000507510.1:p.Pro534Leu
ENST00000683994.1:c.1601C>T ENSP00000507181.1:p.Pro534Leu
ENST00000684290.1:c.1601C>T ENSP00000507243.1:p.Pro534Leu
ENST00000684306.1:c.*1514C>T ENSP00000508384.1:n.*1514C>T
ENST00000684341.1:n.1621C>T
ENST00000684383.1:c.*1239C>T ENSP00000506863.1:n.*1239C>T
ENST00000684482.1:c.4070C>T
ENST00000684619.1:c.*1473C>T ENSP00000508088.1:n.*1473C>T
ENST00000684743.1:n.2632C>T
ENST00000260665.12:c.1601C>T MANE Select ENSP00000260665.7:p.Pro534Leu
ENST00000260665.11:c.1601C>T ENSP00000260665.7:p.Pro534Leu
ENST00000467058.1:n.330C>T
NM_133259.3:c.1601C>T NP_573566.2:p.Pro534Leu
XM_006711915.2:c.1523C>T XP_006711978.1:p.Pro508Leu
XM_006711916.2:c.1601C>T XP_006711979.1:p.Pro534Leu
XM_011532473.1:c.1601C>T XP_011530775.1:p.Pro534Leu
XM_011532474.1:c.1601C>T XP_011530776.1:p.Pro534Leu
XM_006711916.3:c.1601C>T XP_006711979.1:p.Pro534Leu
XM_017003117.1:c.1523C>T XP_016858606.1:p.Pro508Leu
XR_002958896.1:n.1643C>T
NM_133259.4:c.1601C>T MANE Select NP_573566.2:p.Pro534Leu