Canonical Allele Identifier: CA46460072

Gene: LRPPRC

Linked Data

• dbSNP Id: rs201611890
• gnomAD v4: 2-43945334-T-C
• MyVariant Identifiers: chr2:g.44172473T>C (hg19) ; chr2:g.43945334T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43945334T>C , CM000664.2:g.43945334T>C	GRCh38
NC_000002.11:g.44172473T>C , CM000664.1:g.44172473T>C	GRCh37
NC_000002.10:g.44025977T>C	NCBI36
NG_008247.1:g.55672A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409659.6:c.2294A>G	ENSP00000386562.2:p.Gln765Arg
ENST00000447246.2:c.2294A>G	ENSP00000403637.2:p.Gln765Arg
ENST00000681961.1:n.2314A>G
ENST00000682104.1:c.2168A>G	ENSP00000507716.1:p.Gln723Arg
ENST00000682303.1:c.*2082+779A>G	ENSP00000508325.1:n.*2082+779A>G
ENST00000682308.1:c.2294A>G	ENSP00000507056.1:p.Gln765Arg
ENST00000682480.1:c.2294A>G	ENSP00000508344.1:p.Gln765Arg
ENST00000682546.1:c.2291A>G	ENSP00000508188.1:p.Gln764Arg
ENST00000682585.1:c.2294A>G	ENSP00000506885.1:p.Gln765Arg
ENST00000682595.1:n.2876A>G
ENST00000682607.1:c.712A>G
ENST00000682779.1:c.2285A>G	ENSP00000507947.1:p.Gln762Arg
ENST00000682885.1:c.2249A>G	ENSP00000508036.1:p.Gln750Arg
ENST00000682933.1:n.2368A>G
ENST00000683072.1:n.2876A>G
ENST00000683125.1:c.2294A>G	ENSP00000507939.1:p.Gln765Arg
ENST00000683213.1:c.2297A>G	ENSP00000507751.1:p.Gln766Arg
ENST00000683220.1:c.2324A>G	ENSP00000507151.1:p.Gln775Arg
ENST00000683329.1:n.3097A>G
ENST00000683346.1:c.*2169A>G	ENSP00000507458.1:n.*2169A>G
ENST00000683459.1:n.2881A>G
ENST00000683590.1:c.2294A>G	ENSP00000506820.1:p.Gln765Arg
ENST00000683623.1:c.2294A>G	ENSP00000507702.1:p.Gln765Arg
ENST00000683645.1:n.2845A>G
ENST00000683694.1:n.1045A>G
ENST00000683796.1:c.*2166A>G	ENSP00000508221.1:n.*2166A>G
ENST00000683802.1:n.5219A>G
ENST00000683833.1:c.2285A>G	ENSP00000506852.1:p.Gln762Arg
ENST00000683934.1:c.2180A>G
ENST00000683989.1:c.2294A>G	ENSP00000507510.1:p.Gln765Arg
ENST00000683994.1:c.2294A>G	ENSP00000507181.1:p.Gln765Arg
ENST00000684290.1:c.2210+779A>G	ENSP00000507243.1:n.2210+779A>G
ENST00000684306.1:c.*2207A>G	ENSP00000508384.1:n.*2207A>G
ENST00000684341.1:n.2314A>G
ENST00000684383.1:c.*1932A>G	ENSP00000506863.1:n.*1932A>G
ENST00000684619.1:c.*2166A>G	ENSP00000508088.1:n.*2166A>G
ENST00000684743.1:n.3325A>G
ENST00000260665.12:c.2294A>G MANE Select	ENSP00000260665.7:p.Gln765Arg
ENST00000260665.11:c.2294A>G	ENSP00000260665.7:p.Gln765Arg
NM_133259.3:c.2294A>G	NP_573566.2:p.Gln765Arg
XM_006711915.2:c.2216A>G	XP_006711978.1:p.Gln739Arg
XM_006711916.2:c.2294A>G	XP_006711979.1:p.Gln765Arg
XM_011532473.1:c.2294A>G	XP_011530775.1:p.Gln765Arg
XM_011532474.1:c.2294A>G	XP_011530776.1:p.Gln765Arg
XM_006711916.3:c.2294A>G	XP_006711979.1:p.Gln765Arg
XM_017003117.1:c.2216A>G	XP_016858606.1:p.Gln739Arg
XR_002958896.1:n.2336A>G
NM_133259.4:c.2294A>G MANE Select	NP_573566.2:p.Gln765Arg