Canonical Allele Identifier: CA425908630

Gene: LRPPRC

Linked Data

• MyVariant Identifiers: chr2:g.44145494T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43918355T>C , CM000664.2:g.43918355T>C	GRCh38
NC_000002.11:g.44145494T>C , CM000664.1:g.44145494T>C	GRCh37
NC_000002.10:g.43998998T>C	NCBI36
NG_008247.1:g.82651A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681993.1:n.492A>G
ENST00000682295.1:c.204A>G	ENSP00000507499.1:p.Lys68=
ENST00000682303.1:c.*2726A>G	ENSP00000508325.1:n.*2726A>G
ENST00000682308.1:c.2940A>G	ENSP00000507056.1:p.Lys980=
ENST00000682480.1:c.2940A>G	ENSP00000508344.1:p.Lys980=
ENST00000682546.1:c.2937A>G	ENSP00000508188.1:p.Lys979=
ENST00000682585.1:c.2940A>G	ENSP00000506885.1:p.Lys980=
ENST00000682595.1:n.3524A>G
ENST00000682607.1:c.1358A>G
ENST00000682779.1:c.2931A>G	ENSP00000507947.1:p.Lys977=
ENST00000682845.1:n.2042A>G
ENST00000682885.1:c.2895A>G	ENSP00000508036.1:p.Lys965=
ENST00000682933.1:n.3014A>G
ENST00000683072.1:n.3524A>G
ENST00000683080.1:n.559A>G
ENST00000683125.1:c.3048A>G	ENSP00000507939.1:p.Lys1016=
ENST00000683213.1:c.2943A>G	ENSP00000507751.1:p.Lys981=
ENST00000683220.1:c.2970A>G	ENSP00000507151.1:p.Lys990=
ENST00000683236.1:c.270A>G	ENSP00000506891.1:n.270A>G
ENST00000683329.1:n.3743A>G
ENST00000683346.1:c.*2815A>G	ENSP00000507458.1:n.*2815A>G
ENST00000683409.1:n.1547A>G
ENST00000683459.1:n.3527A>G
ENST00000683590.1:c.2897-5797A>G	ENSP00000506820.1:n.2897-5797A>G
ENST00000683623.1:c.2847A>G	ENSP00000507702.1:p.Lys949=
ENST00000683645.1:n.3491A>G
ENST00000683796.1:c.*2812A>G	ENSP00000508221.1:n.*2812A>G
ENST00000683802.1:n.5865A>G
ENST00000683833.1:c.2931A>G	ENSP00000506852.1:p.Lys977=
ENST00000683994.1:c.2940A>G	ENSP00000507181.1:p.Lys980=
ENST00000684290.1:c.*476A>G	ENSP00000507243.1:n.*476A>G
ENST00000684306.1:c.*2853A>G	ENSP00000508384.1:n.*2853A>G
ENST00000684341.1:n.2960A>G
ENST00000684383.1:c.*2578A>G	ENSP00000506863.1:n.*2578A>G
ENST00000684619.1:c.*2812A>G	ENSP00000508088.1:n.*2812A>G
ENST00000684705.1:n.61A>G
ENST00000684743.1:n.3971A>G
ENST00000260665.12:c.2940A>G MANE Select	ENSP00000260665.7:p.Lys980=
ENST00000260665.11:c.2940A>G	ENSP00000260665.7:p.Lys980=
NM_133259.3:c.2940A>G	NP_573566.2:p.Lys980=
XM_006711915.2:c.2862A>G	XP_006711978.1:p.Lys954=
XM_006711916.2:c.2940A>G	XP_006711979.1:p.Lys980=
XM_011532473.1:c.2940A>G	XP_011530775.1:p.Lys980=
XM_011532474.1:c.2940A>G	XP_011530776.1:p.Lys980=
XM_006711916.3:c.2940A>G	XP_006711979.1:p.Lys980=
XM_017003117.1:c.2862A>G	XP_016858606.1:p.Lys954=
XR_002958896.1:n.2982A>G
NM_133259.4:c.2940A>G MANE Select	NP_573566.2:p.Lys980=