Canonical Allele Identifier: CA425908474

Gene: LRPPRC

Linked Data

• MyVariant Identifiers: chr2:g.44145195T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43918056T>A , CM000664.2:g.43918056T>A	GRCh38
NC_000002.11:g.44145195T>A , CM000664.1:g.44145195T>A	GRCh37
NC_000002.10:g.43998699T>A	NCBI36
NG_008247.1:g.82950A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681993.1:n.669A>T
ENST00000682295.1:c.303+200A>T	ENSP00000507499.1:n.303+200A>T
ENST00000682303.1:c.*2903A>T	ENSP00000508325.1:n.*2903A>T
ENST00000682308.1:c.3117A>T	ENSP00000507056.1:p.Ile1039=
ENST00000682480.1:c.3135A>T	ENSP00000508344.1:p.Ile1045=
ENST00000682546.1:c.3114A>T	ENSP00000508188.1:p.Ile1038=
ENST00000682585.1:c.3117A>T	ENSP00000506885.1:p.Ile1039=
ENST00000682595.1:n.3701A>T
ENST00000682607.1:c.1535A>T
ENST00000682779.1:c.3108A>T	ENSP00000507947.1:p.Ile1036=
ENST00000682845.1:n.2219A>T
ENST00000682885.1:c.3072A>T	ENSP00000508036.1:p.Ile1024=
ENST00000682933.1:n.3191A>T
ENST00000683072.1:n.3701A>T
ENST00000683080.1:n.736A>T
ENST00000683125.1:c.3225A>T	ENSP00000507939.1:p.Ile1075=
ENST00000683213.1:c.3120A>T	ENSP00000507751.1:p.Ile1040=
ENST00000683220.1:c.3147A>T	ENSP00000507151.1:p.Ile1049=
ENST00000683329.1:n.3920A>T
ENST00000683346.1:c.*2992A>T	ENSP00000507458.1:n.*2992A>T
ENST00000683409.1:n.1724A>T
ENST00000683459.1:n.3704A>T
ENST00000683590.1:c.2897-5498A>T	ENSP00000506820.1:n.2897-5498A>T
ENST00000683623.1:c.3024A>T	ENSP00000507702.1:p.Ile1008=
ENST00000683645.1:n.3668A>T
ENST00000683796.1:c.*2989A>T	ENSP00000508221.1:n.*2989A>T
ENST00000683802.1:n.6042A>T
ENST00000683833.1:c.3108A>T	ENSP00000506852.1:p.Ile1036=
ENST00000683994.1:c.3117A>T	ENSP00000507181.1:p.Ile1039=
ENST00000684290.1:c.*653A>T	ENSP00000507243.1:n.*653A>T
ENST00000684306.1:c.*3030A>T	ENSP00000508384.1:n.*3030A>T
ENST00000684341.1:n.3137A>T
ENST00000684383.1:c.*2755A>T	ENSP00000506863.1:n.*2755A>T
ENST00000684619.1:c.*2989A>T	ENSP00000508088.1:n.*2989A>T
ENST00000684705.1:n.238A>T
ENST00000684743.1:n.4148A>T
ENST00000260665.12:c.3117A>T MANE Select	ENSP00000260665.7:p.Ile1039=
ENST00000260665.11:c.3117A>T	ENSP00000260665.7:p.Ile1039=
NM_133259.3:c.3117A>T	NP_573566.2:p.Ile1039=
XM_006711915.2:c.3039A>T	XP_006711978.1:p.Ile1013=
XM_006711916.2:c.3117A>T	XP_006711979.1:p.Ile1039=
XM_011532473.1:c.3117A>T	XP_011530775.1:p.Ile1039=
XM_011532474.1:c.3117A>T	XP_011530776.1:p.Ile1039=
XM_006711916.3:c.3117A>T	XP_006711979.1:p.Ile1039=
XM_017003117.1:c.3039A>T	XP_016858606.1:p.Ile1013=
XR_002958896.1:n.3159A>T
NM_133259.4:c.3117A>T MANE Select	NP_573566.2:p.Ile1039=