Canonical Allele Identifier: CA346668515

Gene: LRPPRC

Linked Data

• MyVariant Identifiers: chr2:g.44145454T>C (hg19) ; chr2:g.43918315T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43918315T>C , CM000664.2:g.43918315T>C	GRCh38
NC_000002.11:g.44145454T>C , CM000664.1:g.44145454T>C	GRCh37
NC_000002.10:g.43998958T>C	NCBI36
NG_008247.1:g.82691A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681993.1:n.532A>G
ENST00000682295.1:c.244A>G	ENSP00000507499.1:p.Arg82Gly
ENST00000682303.1:c.*2766A>G	ENSP00000508325.1:n.*2766A>G
ENST00000682308.1:c.2980A>G	ENSP00000507056.1:p.Arg994Gly
ENST00000682480.1:c.2980A>G	ENSP00000508344.1:p.Arg994Gly
ENST00000682546.1:c.2977A>G	ENSP00000508188.1:p.Arg993Gly
ENST00000682585.1:c.2980A>G	ENSP00000506885.1:p.Arg994Gly
ENST00000682595.1:n.3564A>G
ENST00000682607.1:c.1398A>G
ENST00000682779.1:c.2971A>G	ENSP00000507947.1:p.Arg991Gly
ENST00000682845.1:n.2082A>G
ENST00000682885.1:c.2935A>G	ENSP00000508036.1:p.Arg979Gly
ENST00000682933.1:n.3054A>G
ENST00000683072.1:n.3564A>G
ENST00000683080.1:n.599A>G
ENST00000683125.1:c.3088A>G	ENSP00000507939.1:p.Arg1030Gly
ENST00000683213.1:c.2983A>G	ENSP00000507751.1:p.Arg995Gly
ENST00000683220.1:c.3010A>G	ENSP00000507151.1:p.Arg1004Gly
ENST00000683236.1:c.310A>G	ENSP00000506891.1:n.310A>G
ENST00000683329.1:n.3783A>G
ENST00000683346.1:c.*2855A>G	ENSP00000507458.1:n.*2855A>G
ENST00000683409.1:n.1587A>G
ENST00000683459.1:n.3567A>G
ENST00000683590.1:c.2897-5757A>G	ENSP00000506820.1:n.2897-5757A>G
ENST00000683623.1:c.2887A>G	ENSP00000507702.1:p.Arg963Gly
ENST00000683645.1:n.3531A>G
ENST00000683796.1:c.*2852A>G	ENSP00000508221.1:n.*2852A>G
ENST00000683802.1:n.5905A>G
ENST00000683833.1:c.2971A>G	ENSP00000506852.1:p.Arg991Gly
ENST00000683994.1:c.2980A>G	ENSP00000507181.1:p.Arg994Gly
ENST00000684290.1:c.*516A>G	ENSP00000507243.1:n.*516A>G
ENST00000684306.1:c.*2893A>G	ENSP00000508384.1:n.*2893A>G
ENST00000684341.1:n.3000A>G
ENST00000684383.1:c.*2618A>G	ENSP00000506863.1:n.*2618A>G
ENST00000684619.1:c.*2852A>G	ENSP00000508088.1:n.*2852A>G
ENST00000684705.1:n.101A>G
ENST00000684743.1:n.4011A>G
ENST00000260665.12:c.2980A>G MANE Select	ENSP00000260665.7:p.Arg994Gly
ENST00000260665.11:c.2980A>G	ENSP00000260665.7:p.Arg994Gly
NM_133259.3:c.2980A>G	NP_573566.2:p.Arg994Gly
XM_006711915.2:c.2902A>G	XP_006711978.1:p.Arg968Gly
XM_006711916.2:c.2980A>G	XP_006711979.1:p.Arg994Gly
XM_011532473.1:c.2980A>G	XP_011530775.1:p.Arg994Gly
XM_011532474.1:c.2980A>G	XP_011530776.1:p.Arg994Gly
XM_006711916.3:c.2980A>G	XP_006711979.1:p.Arg994Gly
XM_017003117.1:c.2902A>G	XP_016858606.1:p.Arg968Gly
XR_002958896.1:n.3022A>G
NM_133259.4:c.2980A>G MANE Select	NP_573566.2:p.Arg994Gly