Canonical Allele Identifier: CA425908504

Gene: LRPPRC

Linked Data

• MyVariant Identifiers: chr2:g.44145225T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43918086T>C , CM000664.2:g.43918086T>C	GRCh38
NC_000002.11:g.44145225T>C , CM000664.1:g.44145225T>C	GRCh37
NC_000002.10:g.43998729T>C	NCBI36
NG_008247.1:g.82920A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681993.1:n.639A>G
ENST00000682295.1:c.303+170A>G	ENSP00000507499.1:n.303+170A>G
ENST00000682303.1:c.*2873A>G	ENSP00000508325.1:n.*2873A>G
ENST00000682308.1:c.3087A>G	ENSP00000507056.1:p.Ser1029=
ENST00000682480.1:c.3105A>G	ENSP00000508344.1:p.Ser1035=
ENST00000682546.1:c.3084A>G	ENSP00000508188.1:p.Ser1028=
ENST00000682585.1:c.3087A>G	ENSP00000506885.1:p.Ser1029=
ENST00000682595.1:n.3671A>G
ENST00000682607.1:c.1505A>G
ENST00000682779.1:c.3078A>G	ENSP00000507947.1:p.Ser1026=
ENST00000682845.1:n.2189A>G
ENST00000682885.1:c.3042A>G	ENSP00000508036.1:p.Ser1014=
ENST00000682933.1:n.3161A>G
ENST00000683072.1:n.3671A>G
ENST00000683080.1:n.706A>G
ENST00000683125.1:c.3195A>G	ENSP00000507939.1:p.Ser1065=
ENST00000683213.1:c.3090A>G	ENSP00000507751.1:p.Ser1030=
ENST00000683220.1:c.3117A>G	ENSP00000507151.1:p.Ser1039=
ENST00000683329.1:n.3890A>G
ENST00000683346.1:c.*2962A>G	ENSP00000507458.1:n.*2962A>G
ENST00000683409.1:n.1694A>G
ENST00000683459.1:n.3674A>G
ENST00000683590.1:c.2897-5528A>G	ENSP00000506820.1:n.2897-5528A>G
ENST00000683623.1:c.2994A>G	ENSP00000507702.1:p.Ser998=
ENST00000683645.1:n.3638A>G
ENST00000683796.1:c.*2959A>G	ENSP00000508221.1:n.*2959A>G
ENST00000683802.1:n.6012A>G
ENST00000683833.1:c.3078A>G	ENSP00000506852.1:p.Ser1026=
ENST00000683994.1:c.3087A>G	ENSP00000507181.1:p.Ser1029=
ENST00000684290.1:c.*623A>G	ENSP00000507243.1:n.*623A>G
ENST00000684306.1:c.*3000A>G	ENSP00000508384.1:n.*3000A>G
ENST00000684341.1:n.3107A>G
ENST00000684383.1:c.*2725A>G	ENSP00000506863.1:n.*2725A>G
ENST00000684619.1:c.*2959A>G	ENSP00000508088.1:n.*2959A>G
ENST00000684705.1:n.208A>G
ENST00000684743.1:n.4118A>G
ENST00000260665.12:c.3087A>G MANE Select	ENSP00000260665.7:p.Ser1029=
ENST00000260665.11:c.3087A>G	ENSP00000260665.7:p.Ser1029=
NM_133259.3:c.3087A>G	NP_573566.2:p.Ser1029=
XM_006711915.2:c.3009A>G	XP_006711978.1:p.Ser1003=
XM_006711916.2:c.3087A>G	XP_006711979.1:p.Ser1029=
XM_011532473.1:c.3087A>G	XP_011530775.1:p.Ser1029=
XM_011532474.1:c.3087A>G	XP_011530776.1:p.Ser1029=
XM_006711916.3:c.3087A>G	XP_006711979.1:p.Ser1029=
XM_017003117.1:c.3009A>G	XP_016858606.1:p.Ser1003=
XR_002958896.1:n.3129A>G
NM_133259.4:c.3087A>G MANE Select	NP_573566.2:p.Ser1029=