Canonical Allele Identifier: CA425909728

Gene: LRPPRC

Linked Data

• MyVariant Identifiers: chr2:g.44170909C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43943770C>T , CM000664.2:g.43943770C>T	GRCh38
NC_000002.11:g.44170909C>T , CM000664.1:g.44170909C>T	GRCh37
NC_000002.10:g.44024413C>T	NCBI36
NG_008247.1:g.57236G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000409659.6:c.2421G>A	ENSP00000386562.2:p.Gln807=
ENST00000447246.2:c.2421G>A	ENSP00000403637.2:p.Gln807=
ENST00000681961.1:n.2441G>A
ENST00000682104.1:c.2295G>A	ENSP00000507716.1:p.Gln765=
ENST00000682303.1:c.*2207G>A	ENSP00000508325.1:n.*2207G>A
ENST00000682308.1:c.2421G>A	ENSP00000507056.1:p.Gln807=
ENST00000682480.1:c.2421G>A	ENSP00000508344.1:p.Gln807=
ENST00000682546.1:c.2418G>A	ENSP00000508188.1:p.Gln806=
ENST00000682585.1:c.2421G>A	ENSP00000506885.1:p.Gln807=
ENST00000682595.1:n.3003G>A
ENST00000682607.1:c.839G>A
ENST00000682779.1:c.2412G>A	ENSP00000507947.1:p.Gln804=
ENST00000682845.1:n.1523G>A
ENST00000682885.1:c.2376G>A	ENSP00000508036.1:p.Gln792=
ENST00000682933.1:n.2495G>A
ENST00000683072.1:n.3003G>A
ENST00000683125.1:c.2421G>A	ENSP00000507939.1:p.Gln807=
ENST00000683213.1:c.2424G>A	ENSP00000507751.1:p.Gln808=
ENST00000683220.1:c.2451G>A	ENSP00000507151.1:p.Gln817=
ENST00000683329.1:n.3224G>A
ENST00000683346.1:c.*2296G>A	ENSP00000507458.1:n.*2296G>A
ENST00000683459.1:n.3008G>A
ENST00000683590.1:c.2421G>A	ENSP00000506820.1:p.Gln807=
ENST00000683623.1:c.2328G>A	ENSP00000507702.1:p.Gln776=
ENST00000683645.1:n.2972G>A
ENST00000683694.1:n.1172G>A
ENST00000683796.1:c.*2293G>A	ENSP00000508221.1:n.*2293G>A
ENST00000683802.1:n.5346G>A
ENST00000683833.1:c.2412G>A	ENSP00000506852.1:p.Gln804=
ENST00000683989.1:c.2421G>A	ENSP00000507510.1:p.Gln807=
ENST00000683994.1:c.2421G>A	ENSP00000507181.1:p.Gln807=
ENST00000684290.1:c.*115G>A	ENSP00000507243.1:n.*115G>A
ENST00000684306.1:c.*2334G>A	ENSP00000508384.1:n.*2334G>A
ENST00000684341.1:n.2441G>A
ENST00000684383.1:c.*2059G>A	ENSP00000506863.1:n.*2059G>A
ENST00000684397.1:c.125G>A
ENST00000684619.1:c.*2293G>A	ENSP00000508088.1:n.*2293G>A
ENST00000684743.1:n.3452G>A
ENST00000260665.12:c.2421G>A MANE Select	ENSP00000260665.7:p.Gln807=
ENST00000260665.11:c.2421G>A	ENSP00000260665.7:p.Gln807=
NM_133259.3:c.2421G>A	NP_573566.2:p.Gln807=
XM_006711915.2:c.2343G>A	XP_006711978.1:p.Gln781=
XM_006711916.2:c.2421G>A	XP_006711979.1:p.Gln807=
XM_011532473.1:c.2421G>A	XP_011530775.1:p.Gln807=
XM_011532474.1:c.2421G>A	XP_011530776.1:p.Gln807=
XM_006711916.3:c.2421G>A	XP_006711979.1:p.Gln807=
XM_017003117.1:c.2343G>A	XP_016858606.1:p.Gln781=
XR_002958896.1:n.2463G>A
NM_133259.4:c.2421G>A MANE Select	NP_573566.2:p.Gln807=