Canonical Allele Identifier: CA346665090

Gene: LRPPRC

Linked Data

• MyVariant Identifiers: chr2:g.44132902T>A (hg19) ; chr2:g.43905763T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43905763T>A , CM000664.2:g.43905763T>A	GRCh38
NC_000002.11:g.44132902T>A , CM000664.1:g.44132902T>A	GRCh37
NC_000002.10:g.43986406T>A	NCBI36
NG_008247.1:g.95243A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000472420.6:n.372A>T
ENST00000681993.1:n.845A>T
ENST00000682295.1:c.448A>T	ENSP00000507499.1:n.448A>T
ENST00000682303.1:c.*3079A>T	ENSP00000508325.1:n.*3079A>T
ENST00000682308.1:c.3293A>T	ENSP00000507056.1:p.Lys1098Met
ENST00000682480.1:c.3311A>T	ENSP00000508344.1:p.Lys1104Met
ENST00000682546.1:c.3290A>T	ENSP00000508188.1:p.Lys1097Met
ENST00000682585.1:c.3293A>T	ENSP00000506885.1:p.Lys1098Met
ENST00000682595.1:n.3877A>T
ENST00000682607.1:c.1711A>T
ENST00000682612.1:c.145A>T
ENST00000682779.1:c.3284A>T	ENSP00000507947.1:p.Lys1095Met
ENST00000682845.1:n.2395A>T
ENST00000682885.1:c.3248A>T	ENSP00000508036.1:p.Lys1083Met
ENST00000682933.1:n.3367A>T
ENST00000683002.1:c.145A>T
ENST00000683072.1:n.3877A>T
ENST00000683080.1:n.912A>T
ENST00000683125.1:c.3401A>T	ENSP00000507939.1:p.Lys1134Met
ENST00000683213.1:c.3296A>T	ENSP00000507751.1:p.Lys1099Met
ENST00000683220.1:c.3323A>T	ENSP00000507151.1:p.Lys1108Met
ENST00000683329.1:n.4096A>T
ENST00000683346.1:c.*3168A>T	ENSP00000507458.1:n.*3168A>T
ENST00000683409.1:n.1900A>T
ENST00000683459.1:n.3880A>T
ENST00000683528.1:c.145A>T
ENST00000683590.1:c.3041A>T	ENSP00000506820.1:p.Lys1014Met
ENST00000683623.1:c.3200A>T	ENSP00000507702.1:p.Lys1067Met
ENST00000683645.1:n.3844A>T
ENST00000683796.1:c.*3165A>T	ENSP00000508221.1:n.*3165A>T
ENST00000683802.1:n.6218A>T
ENST00000683833.1:c.3284A>T	ENSP00000506852.1:p.Lys1095Met
ENST00000683994.1:c.3293A>T	ENSP00000507181.1:p.Lys1098Met
ENST00000684290.1:c.*829A>T	ENSP00000507243.1:n.*829A>T
ENST00000684306.1:c.*3206A>T	ENSP00000508384.1:n.*3206A>T
ENST00000684341.1:n.3313A>T
ENST00000684383.1:c.*2931A>T	ENSP00000506863.1:n.*2931A>T
ENST00000684418.1:n.4474A>T
ENST00000684454.1:n.2643A>T
ENST00000684619.1:c.*3165A>T	ENSP00000508088.1:n.*3165A>T
ENST00000684743.1:n.4324A>T
ENST00000260665.12:c.3293A>T MANE Select	ENSP00000260665.7:p.Lys1098Met
ENST00000260665.11:c.3293A>T	ENSP00000260665.7:p.Lys1098Met
NM_133259.3:c.3293A>T	NP_573566.2:p.Lys1098Met
XM_006711915.2:c.3215A>T	XP_006711978.1:p.Lys1072Met
XM_011532473.1:c.3293A>T	XP_011530775.1:p.Lys1098Met
XM_011532474.1:c.3293A>T	XP_011530776.1:p.Lys1098Met
XM_017003117.1:c.3215A>T	XP_016858606.1:p.Lys1072Met
XR_002958896.1:n.3335A>T
NM_133259.4:c.3293A>T MANE Select	NP_573566.2:p.Lys1098Met