Canonical Allele Identifier: CA346668677

Gene: LRPPRC

Linked Data

• MyVariant Identifiers: chr2:g.44145529C>G (hg19) ; chr2:g.43918390C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43918390C>G , CM000664.2:g.43918390C>G	GRCh38
NC_000002.11:g.44145529C>G , CM000664.1:g.44145529C>G	GRCh37
NC_000002.10:g.43999033C>G	NCBI36
NG_008247.1:g.82616G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681993.1:n.457G>C
ENST00000682295.1:c.169G>C	ENSP00000507499.1:p.Gly57Arg
ENST00000682303.1:c.*2691G>C	ENSP00000508325.1:n.*2691G>C
ENST00000682308.1:c.2905G>C	ENSP00000507056.1:p.Gly969Arg
ENST00000682480.1:c.2905G>C	ENSP00000508344.1:p.Gly969Arg
ENST00000682546.1:c.2902G>C	ENSP00000508188.1:p.Gly968Arg
ENST00000682585.1:c.2905G>C	ENSP00000506885.1:p.Gly969Arg
ENST00000682595.1:n.3489G>C
ENST00000682607.1:c.1323G>C
ENST00000682779.1:c.2896G>C	ENSP00000507947.1:p.Gly966Arg
ENST00000682845.1:n.2007G>C
ENST00000682885.1:c.2860G>C	ENSP00000508036.1:p.Gly954Arg
ENST00000682933.1:n.2979G>C
ENST00000683072.1:n.3489G>C
ENST00000683080.1:n.524G>C
ENST00000683125.1:c.3013G>C	ENSP00000507939.1:p.Gly1005Arg
ENST00000683213.1:c.2908G>C	ENSP00000507751.1:p.Gly970Arg
ENST00000683220.1:c.2935G>C	ENSP00000507151.1:p.Gly979Arg
ENST00000683236.1:c.235G>C	ENSP00000506891.1:n.235G>C
ENST00000683329.1:n.3708G>C
ENST00000683346.1:c.*2780G>C	ENSP00000507458.1:n.*2780G>C
ENST00000683409.1:n.1512G>C
ENST00000683459.1:n.3492G>C
ENST00000683590.1:c.2897-5832G>C	ENSP00000506820.1:n.2897-5832G>C
ENST00000683623.1:c.2812G>C	ENSP00000507702.1:p.Gly938Arg
ENST00000683645.1:n.3456G>C
ENST00000683796.1:c.*2777G>C	ENSP00000508221.1:n.*2777G>C
ENST00000683802.1:n.5830G>C
ENST00000683833.1:c.2896G>C	ENSP00000506852.1:p.Gly966Arg
ENST00000683994.1:c.2905G>C	ENSP00000507181.1:p.Gly969Arg
ENST00000684290.1:c.*441G>C	ENSP00000507243.1:n.*441G>C
ENST00000684306.1:c.*2818G>C	ENSP00000508384.1:n.*2818G>C
ENST00000684341.1:n.2925G>C
ENST00000684383.1:c.*2543G>C	ENSP00000506863.1:n.*2543G>C
ENST00000684619.1:c.*2777G>C	ENSP00000508088.1:n.*2777G>C
ENST00000684705.1:n.26G>C
ENST00000684743.1:n.3936G>C
ENST00000260665.12:c.2905G>C MANE Select	ENSP00000260665.7:p.Gly969Arg
ENST00000260665.11:c.2905G>C	ENSP00000260665.7:p.Gly969Arg
NM_133259.3:c.2905G>C	NP_573566.2:p.Gly969Arg
XM_006711915.2:c.2827G>C	XP_006711978.1:p.Gly943Arg
XM_006711916.2:c.2905G>C	XP_006711979.1:p.Gly969Arg
XM_011532473.1:c.2905G>C	XP_011530775.1:p.Gly969Arg
XM_011532474.1:c.2905G>C	XP_011530776.1:p.Gly969Arg
XM_006711916.3:c.2905G>C	XP_006711979.1:p.Gly969Arg
XM_017003117.1:c.2827G>C	XP_016858606.1:p.Gly943Arg
XR_002958896.1:n.2947G>C
NM_133259.4:c.2905G>C MANE Select	NP_573566.2:p.Gly969Arg