Canonical Allele Identifier: CA346672780

Gene: LRPPRC

Linked Data

• MyVariant Identifiers: chr2:g.44170916A>G (hg19) ; chr2:g.43943777A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43943777A>G , CM000664.2:g.43943777A>G	GRCh38
NC_000002.11:g.44170916A>G , CM000664.1:g.44170916A>G	GRCh37
NC_000002.10:g.44024420A>G	NCBI36
NG_008247.1:g.57229T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000409659.6:c.2414T>C	ENSP00000386562.2:p.Val805Ala
ENST00000447246.2:c.2414T>C	ENSP00000403637.2:p.Val805Ala
ENST00000681961.1:n.2434T>C
ENST00000682104.1:c.2288T>C	ENSP00000507716.1:p.Val763Ala
ENST00000682303.1:c.*2200T>C	ENSP00000508325.1:n.*2200T>C
ENST00000682308.1:c.2414T>C	ENSP00000507056.1:p.Val805Ala
ENST00000682480.1:c.2414T>C	ENSP00000508344.1:p.Val805Ala
ENST00000682546.1:c.2411T>C	ENSP00000508188.1:p.Val804Ala
ENST00000682585.1:c.2414T>C	ENSP00000506885.1:p.Val805Ala
ENST00000682595.1:n.2996T>C
ENST00000682607.1:c.832T>C
ENST00000682779.1:c.2405T>C	ENSP00000507947.1:p.Val802Ala
ENST00000682845.1:n.1516T>C
ENST00000682885.1:c.2369T>C	ENSP00000508036.1:p.Val790Ala
ENST00000682933.1:n.2488T>C
ENST00000683072.1:n.2996T>C
ENST00000683125.1:c.2414T>C	ENSP00000507939.1:p.Val805Ala
ENST00000683213.1:c.2417T>C	ENSP00000507751.1:p.Val806Ala
ENST00000683220.1:c.2444T>C	ENSP00000507151.1:p.Val815Ala
ENST00000683329.1:n.3217T>C
ENST00000683346.1:c.*2289T>C	ENSP00000507458.1:n.*2289T>C
ENST00000683459.1:n.3001T>C
ENST00000683590.1:c.2414T>C	ENSP00000506820.1:p.Val805Ala
ENST00000683623.1:c.2321T>C	ENSP00000507702.1:p.Val774Ala
ENST00000683645.1:n.2965T>C
ENST00000683694.1:n.1165T>C
ENST00000683796.1:c.*2286T>C	ENSP00000508221.1:n.*2286T>C
ENST00000683802.1:n.5339T>C
ENST00000683833.1:c.2405T>C	ENSP00000506852.1:p.Val802Ala
ENST00000683989.1:c.2414T>C	ENSP00000507510.1:p.Val805Ala
ENST00000683994.1:c.2414T>C	ENSP00000507181.1:p.Val805Ala
ENST00000684290.1:c.*108T>C	ENSP00000507243.1:n.*108T>C
ENST00000684306.1:c.*2327T>C	ENSP00000508384.1:n.*2327T>C
ENST00000684341.1:n.2434T>C
ENST00000684383.1:c.*2052T>C	ENSP00000506863.1:n.*2052T>C
ENST00000684397.1:c.118T>C
ENST00000684619.1:c.*2286T>C	ENSP00000508088.1:n.*2286T>C
ENST00000684743.1:n.3445T>C
ENST00000260665.12:c.2414T>C MANE Select	ENSP00000260665.7:p.Val805Ala
ENST00000260665.11:c.2414T>C	ENSP00000260665.7:p.Val805Ala
NM_133259.3:c.2414T>C	NP_573566.2:p.Val805Ala
XM_006711915.2:c.2336T>C	XP_006711978.1:p.Val779Ala
XM_006711916.2:c.2414T>C	XP_006711979.1:p.Val805Ala
XM_011532473.1:c.2414T>C	XP_011530775.1:p.Val805Ala
XM_011532474.1:c.2414T>C	XP_011530776.1:p.Val805Ala
XM_006711916.3:c.2414T>C	XP_006711979.1:p.Val805Ala
XM_017003117.1:c.2336T>C	XP_016858606.1:p.Val779Ala
XR_002958896.1:n.2456T>C
NM_133259.4:c.2414T>C MANE Select	NP_573566.2:p.Val805Ala