Canonical Allele Identifier: CA425909739

Gene: LRPPRC

Linked Data

• MyVariant Identifiers: chr2:g.44170918T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43943779T>C , CM000664.2:g.43943779T>C	GRCh38
NC_000002.11:g.44170918T>C , CM000664.1:g.44170918T>C	GRCh37
NC_000002.10:g.44024422T>C	NCBI36
NG_008247.1:g.57227A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000409659.6:c.2412A>G	ENSP00000386562.2:p.Thr804=
ENST00000447246.2:c.2412A>G	ENSP00000403637.2:p.Thr804=
ENST00000681961.1:n.2432A>G
ENST00000682104.1:c.2286A>G	ENSP00000507716.1:p.Thr762=
ENST00000682303.1:c.*2198A>G	ENSP00000508325.1:n.*2198A>G
ENST00000682308.1:c.2412A>G	ENSP00000507056.1:p.Thr804=
ENST00000682480.1:c.2412A>G	ENSP00000508344.1:p.Thr804=
ENST00000682546.1:c.2409A>G	ENSP00000508188.1:p.Thr803=
ENST00000682585.1:c.2412A>G	ENSP00000506885.1:p.Thr804=
ENST00000682595.1:n.2994A>G
ENST00000682607.1:c.830A>G
ENST00000682779.1:c.2403A>G	ENSP00000507947.1:p.Thr801=
ENST00000682845.1:n.1514A>G
ENST00000682885.1:c.2367A>G	ENSP00000508036.1:p.Thr789=
ENST00000682933.1:n.2486A>G
ENST00000683072.1:n.2994A>G
ENST00000683125.1:c.2412A>G	ENSP00000507939.1:p.Thr804=
ENST00000683213.1:c.2415A>G	ENSP00000507751.1:p.Thr805=
ENST00000683220.1:c.2442A>G	ENSP00000507151.1:p.Thr814=
ENST00000683329.1:n.3215A>G
ENST00000683346.1:c.*2287A>G	ENSP00000507458.1:n.*2287A>G
ENST00000683459.1:n.2999A>G
ENST00000683590.1:c.2412A>G	ENSP00000506820.1:p.Thr804=
ENST00000683623.1:c.2319A>G	ENSP00000507702.1:p.Thr773=
ENST00000683645.1:n.2963A>G
ENST00000683694.1:n.1163A>G
ENST00000683796.1:c.*2284A>G	ENSP00000508221.1:n.*2284A>G
ENST00000683802.1:n.5337A>G
ENST00000683833.1:c.2403A>G	ENSP00000506852.1:p.Thr801=
ENST00000683989.1:c.2412A>G	ENSP00000507510.1:p.Thr804=
ENST00000683994.1:c.2412A>G	ENSP00000507181.1:p.Thr804=
ENST00000684290.1:c.*106A>G	ENSP00000507243.1:n.*106A>G
ENST00000684306.1:c.*2325A>G	ENSP00000508384.1:n.*2325A>G
ENST00000684341.1:n.2432A>G
ENST00000684383.1:c.*2050A>G	ENSP00000506863.1:n.*2050A>G
ENST00000684397.1:c.116A>G
ENST00000684619.1:c.*2284A>G	ENSP00000508088.1:n.*2284A>G
ENST00000684743.1:n.3443A>G
ENST00000260665.12:c.2412A>G MANE Select	ENSP00000260665.7:p.Thr804=
ENST00000260665.11:c.2412A>G	ENSP00000260665.7:p.Thr804=
NM_133259.3:c.2412A>G	NP_573566.2:p.Thr804=
XM_006711915.2:c.2334A>G	XP_006711978.1:p.Thr778=
XM_006711916.2:c.2412A>G	XP_006711979.1:p.Thr804=
XM_011532473.1:c.2412A>G	XP_011530775.1:p.Thr804=
XM_011532474.1:c.2412A>G	XP_011530776.1:p.Thr804=
XM_006711916.3:c.2412A>G	XP_006711979.1:p.Thr804=
XM_017003117.1:c.2334A>G	XP_016858606.1:p.Thr778=
XR_002958896.1:n.2454A>G
NM_133259.4:c.2412A>G MANE Select	NP_573566.2:p.Thr804=