Canonical Allele Identifier: CA346676159

Gene: LRPPRC

Linked Data

• MyVariant Identifiers: chr2:g.44175316A>C (hg19) ; chr2:g.43948177A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43948177A>C , CM000664.2:g.43948177A>C	GRCh38
NC_000002.11:g.44175316A>C , CM000664.1:g.44175316A>C	GRCh37
NC_000002.10:g.44028820A>C	NCBI36
NG_008247.1:g.52829T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409659.6:c.1865T>G	ENSP00000386562.2:p.Ile622Ser
ENST00000447246.2:c.1865T>G	ENSP00000403637.2:p.Ile622Ser
ENST00000467058.2:n.594T>G
ENST00000681959.1:n.1479T>G
ENST00000681961.1:n.1885T>G
ENST00000682104.1:c.1739T>G	ENSP00000507716.1:p.Ile580Ser
ENST00000682303.1:c.*1737T>G	ENSP00000508325.1:n.*1737T>G
ENST00000682308.1:c.1865T>G	ENSP00000507056.1:p.Ile622Ser
ENST00000682480.1:c.1865T>G	ENSP00000508344.1:p.Ile622Ser
ENST00000682546.1:c.1862T>G	ENSP00000508188.1:p.Ile621Ser
ENST00000682585.1:c.1865T>G	ENSP00000506885.1:p.Ile622Ser
ENST00000682595.1:n.2447T>G
ENST00000682607.1:c.283T>G
ENST00000682779.1:c.1856T>G	ENSP00000507947.1:p.Ile619Ser
ENST00000682885.1:c.1865T>G	ENSP00000508036.1:p.Ile622Ser
ENST00000682933.1:n.1939T>G
ENST00000683072.1:n.2447T>G
ENST00000683082.1:n.1883T>G
ENST00000683125.1:c.1865T>G	ENSP00000507939.1:p.Ile622Ser
ENST00000683213.1:c.1868T>G	ENSP00000507751.1:p.Ile623Ser
ENST00000683220.1:c.1895T>G	ENSP00000507151.1:p.Ile632Ser
ENST00000683329.1:n.2668T>G
ENST00000683346.1:c.*1740T>G	ENSP00000507458.1:n.*1740T>G
ENST00000683459.1:n.2452T>G
ENST00000683590.1:c.1865T>G	ENSP00000506820.1:p.Ile622Ser
ENST00000683623.1:c.1865T>G	ENSP00000507702.1:p.Ile622Ser
ENST00000683645.1:n.2416T>G
ENST00000683694.1:n.616T>G
ENST00000683796.1:c.*1737T>G	ENSP00000508221.1:n.*1737T>G
ENST00000683802.1:n.4790T>G
ENST00000683833.1:c.1856T>G	ENSP00000506852.1:p.Ile619Ser
ENST00000683934.1:c.1751T>G
ENST00000683989.1:c.1865T>G	ENSP00000507510.1:p.Ile622Ser
ENST00000683994.1:c.1865T>G	ENSP00000507181.1:p.Ile622Ser
ENST00000684290.1:c.1865T>G	ENSP00000507243.1:p.Ile622Ser
ENST00000684306.1:c.*1778T>G	ENSP00000508384.1:n.*1778T>G
ENST00000684341.1:n.1885T>G
ENST00000684383.1:c.*1503T>G	ENSP00000506863.1:n.*1503T>G
ENST00000684482.1:c.4334T>G
ENST00000684619.1:c.*1737T>G	ENSP00000508088.1:n.*1737T>G
ENST00000684743.1:n.2896T>G
ENST00000260665.12:c.1865T>G MANE Select	ENSP00000260665.7:p.Ile622Ser
ENST00000260665.11:c.1865T>G	ENSP00000260665.7:p.Ile622Ser
NM_133259.3:c.1865T>G	NP_573566.2:p.Ile622Ser
XM_006711915.2:c.1787T>G	XP_006711978.1:p.Ile596Ser
XM_006711916.2:c.1865T>G	XP_006711979.1:p.Ile622Ser
XM_011532473.1:c.1865T>G	XP_011530775.1:p.Ile622Ser
XM_011532474.1:c.1865T>G	XP_011530776.1:p.Ile622Ser
XM_006711916.3:c.1865T>G	XP_006711979.1:p.Ile622Ser
XM_017003117.1:c.1787T>G	XP_016858606.1:p.Ile596Ser
XR_002958896.1:n.1907T>G
NM_133259.4:c.1865T>G MANE Select	NP_573566.2:p.Ile622Ser