Canonical Allele Identifier: CA532288068

Gene: LRPPRC

Linked Data

• dbSNP Id: rs1414406467
• gnomAD v2: 2-44184411-T-G
• gnomAD v3: 2-43957272-T-G
• gnomAD v4: 2-43957272-T-G
• MyVariant Identifiers: chr2:g.44184411T>G (hg19) ; chr2:g.43957272T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43957272T>G , CM000664.2:g.43957272T>G	GRCh38
NC_000002.11:g.44184411T>G , CM000664.1:g.44184411T>G	GRCh37
NC_000002.10:g.44037915T>G	NCBI36
NG_008247.1:g.43734A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409659.6:c.1649+113A>C	ENSP00000386562.2:n.1649+113A>C
ENST00000447246.2:c.1649+113A>C	ENSP00000403637.2:n.1649+113A>C
ENST00000467058.2:n.378+113A>C
ENST00000681959.1:n.1263+113A>C
ENST00000681961.1:n.1669+113A>C
ENST00000682104.1:c.1523+113A>C	ENSP00000507716.1:n.1523+113A>C
ENST00000682303.1:c.*1521+113A>C	ENSP00000508325.1:n.*1521+113A>C
ENST00000682308.1:c.1649+113A>C	ENSP00000507056.1:n.1649+113A>C
ENST00000682480.1:c.1649+113A>C	ENSP00000508344.1:n.1649+113A>C
ENST00000682546.1:c.1649+113A>C	ENSP00000508188.1:n.1649+113A>C
ENST00000682585.1:c.1649+113A>C	ENSP00000506885.1:n.1649+113A>C
ENST00000682595.1:n.2231+113A>C
ENST00000682607.1:c.67+113A>C
ENST00000682779.1:c.1640+113A>C	ENSP00000507947.1:n.1640+113A>C
ENST00000682885.1:c.1649+113A>C	ENSP00000508036.1:n.1649+113A>C
ENST00000682933.1:n.1723+113A>C
ENST00000683072.1:n.2231+113A>C
ENST00000683082.1:n.1667+113A>C
ENST00000683125.1:c.1649+113A>C	ENSP00000507939.1:n.1649+113A>C
ENST00000683213.1:c.1652+113A>C	ENSP00000507751.1:n.1652+113A>C
ENST00000683220.1:c.1649+113A>C	ENSP00000507151.1:n.1649+113A>C
ENST00000683329.1:n.2452+113A>C
ENST00000683346.1:c.*1524+113A>C	ENSP00000507458.1:n.*1524+113A>C
ENST00000683459.1:n.2236+113A>C
ENST00000683590.1:c.1649+113A>C	ENSP00000506820.1:n.1649+113A>C
ENST00000683623.1:c.1649+113A>C	ENSP00000507702.1:n.1649+113A>C
ENST00000683645.1:n.2169+113A>C
ENST00000683694.1:n.400+113A>C
ENST00000683796.1:c.*1521+113A>C	ENSP00000508221.1:n.*1521+113A>C
ENST00000683802.1:n.4574+113A>C
ENST00000683833.1:c.1640+113A>C	ENSP00000506852.1:n.1640+113A>C
ENST00000683934.1:c.1535+113A>C
ENST00000683989.1:c.1649+113A>C	ENSP00000507510.1:n.1649+113A>C
ENST00000683994.1:c.1649+113A>C	ENSP00000507181.1:n.1649+113A>C
ENST00000684290.1:c.1649+113A>C	ENSP00000507243.1:n.1649+113A>C
ENST00000684306.1:c.*1562+113A>C	ENSP00000508384.1:n.*1562+113A>C
ENST00000684341.1:n.1669+113A>C
ENST00000684383.1:c.*1287+113A>C	ENSP00000506863.1:n.*1287+113A>C
ENST00000684482.1:c.4118+113A>C
ENST00000684619.1:c.*1521+113A>C	ENSP00000508088.1:n.*1521+113A>C
ENST00000684743.1:n.2680+113A>C
ENST00000260665.12:c.1649+113A>C MANE Select	ENSP00000260665.7:n.1649+113A>C
ENST00000260665.11:c.1649+113A>C	ENSP00000260665.7:n.1649+113A>C
ENST00000467058.1:n.378+113A>C
NM_133259.3:c.1649+113A>C	NP_573566.2:n.1649+113A>C
XM_006711915.2:c.1571+113A>C	XP_006711978.1:n.1571+113A>C
XM_006711916.2:c.1649+113A>C	XP_006711979.1:n.1649+113A>C
XM_011532473.1:c.1649+113A>C	XP_011530775.1:n.1649+113A>C
XM_011532474.1:c.1649+113A>C	XP_011530776.1:n.1649+113A>C
XM_006711916.3:c.1649+113A>C	XP_006711979.1:n.1649+113A>C
XM_017003117.1:c.1571+113A>C	XP_016858606.1:n.1571+113A>C
XR_002958896.1:n.1691+113A>C
NM_133259.4:c.1649+113A>C MANE Select	NP_573566.2:n.1649+113A>C