Canonical Allele Identifier: CA346678568

Gene: LRPPRC

Linked Data

• MyVariant Identifiers: chr2:g.44184572G>C (hg19) ; chr2:g.43957433G>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409659.6:c.1601C>G	ENSP00000386562.2:p.Pro534Arg
ENST00000447246.2:c.1601C>G	ENSP00000403637.2:p.Pro534Arg
ENST00000467058.2:n.330C>G
ENST00000681959.1:n.1215C>G
ENST00000681961.1:n.1621C>G
ENST00000682104.1:c.1475C>G	ENSP00000507716.1:p.Pro492Arg
ENST00000682303.1:c.*1473C>G	ENSP00000508325.1:n.*1473C>G
ENST00000682308.1:c.1601C>G	ENSP00000507056.1:p.Pro534Arg
ENST00000682480.1:c.1601C>G	ENSP00000508344.1:p.Pro534Arg
ENST00000682546.1:c.1601C>G	ENSP00000508188.1:p.Pro534Arg
ENST00000682585.1:c.1601C>G	ENSP00000506885.1:p.Pro534Arg
ENST00000682595.1:n.2183C>G
ENST00000682607.1:c.19C>G
ENST00000682779.1:c.1592C>G	ENSP00000507947.1:p.Pro531Arg
ENST00000682885.1:c.1601C>G	ENSP00000508036.1:p.Pro534Arg
ENST00000682933.1:n.1675C>G
ENST00000683072.1:n.2183C>G
ENST00000683082.1:n.1619C>G
ENST00000683125.1:c.1601C>G	ENSP00000507939.1:p.Pro534Arg
ENST00000683213.1:c.1604C>G	ENSP00000507751.1:p.Pro535Arg
ENST00000683220.1:c.1601C>G	ENSP00000507151.1:p.Pro534Arg
ENST00000683329.1:n.2404C>G
ENST00000683346.1:c.*1476C>G	ENSP00000507458.1:n.*1476C>G
ENST00000683459.1:n.2188C>G
ENST00000683590.1:c.1601C>G	ENSP00000506820.1:p.Pro534Arg
ENST00000683623.1:c.1601C>G	ENSP00000507702.1:p.Pro534Arg
ENST00000683645.1:n.2121C>G
ENST00000683694.1:n.352C>G
ENST00000683796.1:c.*1473C>G	ENSP00000508221.1:n.*1473C>G
ENST00000683802.1:n.4526C>G
ENST00000683833.1:c.1592C>G	ENSP00000506852.1:p.Pro531Arg
ENST00000683934.1:c.1487C>G
ENST00000683989.1:c.1601C>G	ENSP00000507510.1:p.Pro534Arg
ENST00000683994.1:c.1601C>G	ENSP00000507181.1:p.Pro534Arg
ENST00000684290.1:c.1601C>G	ENSP00000507243.1:p.Pro534Arg
ENST00000684306.1:c.*1514C>G	ENSP00000508384.1:n.*1514C>G
ENST00000684341.1:n.1621C>G
ENST00000684383.1:c.*1239C>G	ENSP00000506863.1:n.*1239C>G
ENST00000684482.1:c.4070C>G
ENST00000684619.1:c.*1473C>G	ENSP00000508088.1:n.*1473C>G
ENST00000684743.1:n.2632C>G
ENST00000260665.12:c.1601C>G MANE Select	ENSP00000260665.7:p.Pro534Arg
ENST00000260665.11:c.1601C>G	ENSP00000260665.7:p.Pro534Arg
ENST00000467058.1:n.330C>G
NM_133259.3:c.1601C>G	NP_573566.2:p.Pro534Arg
XM_006711915.2:c.1523C>G	XP_006711978.1:p.Pro508Arg
XM_006711916.2:c.1601C>G	XP_006711979.1:p.Pro534Arg
XM_011532473.1:c.1601C>G	XP_011530775.1:p.Pro534Arg
XM_011532474.1:c.1601C>G	XP_011530776.1:p.Pro534Arg
XM_006711916.3:c.1601C>G	XP_006711979.1:p.Pro534Arg
XM_017003117.1:c.1523C>G	XP_016858606.1:p.Pro508Arg
XR_002958896.1:n.1643C>G
NM_133259.4:c.1601C>G MANE Select	NP_573566.2:p.Pro534Arg