Canonical Allele Identifier: CA346676255

Gene: LRPPRC

Linked Data

• MyVariant Identifiers: chr2:g.44175338T>A (hg19) ; chr2:g.43948199T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43948199T>A , CM000664.2:g.43948199T>A	GRCh38
NC_000002.11:g.44175338T>A , CM000664.1:g.44175338T>A	GRCh37
NC_000002.10:g.44028842T>A	NCBI36
NG_008247.1:g.52807A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409659.6:c.1843A>T	ENSP00000386562.2:p.Asn615Tyr
ENST00000447246.2:c.1843A>T	ENSP00000403637.2:p.Asn615Tyr
ENST00000467058.2:n.572A>T
ENST00000681959.1:n.1457A>T
ENST00000681961.1:n.1863A>T
ENST00000682104.1:c.1717A>T	ENSP00000507716.1:p.Asn573Tyr
ENST00000682303.1:c.*1715A>T	ENSP00000508325.1:n.*1715A>T
ENST00000682308.1:c.1843A>T	ENSP00000507056.1:p.Asn615Tyr
ENST00000682480.1:c.1843A>T	ENSP00000508344.1:p.Asn615Tyr
ENST00000682546.1:c.1840A>T	ENSP00000508188.1:p.Asn614Tyr
ENST00000682585.1:c.1843A>T	ENSP00000506885.1:p.Asn615Tyr
ENST00000682595.1:n.2425A>T
ENST00000682607.1:c.261A>T
ENST00000682779.1:c.1834A>T	ENSP00000507947.1:p.Asn612Tyr
ENST00000682885.1:c.1843A>T	ENSP00000508036.1:p.Asn615Tyr
ENST00000682933.1:n.1917A>T
ENST00000683072.1:n.2425A>T
ENST00000683082.1:n.1861A>T
ENST00000683125.1:c.1843A>T	ENSP00000507939.1:p.Asn615Tyr
ENST00000683213.1:c.1846A>T	ENSP00000507751.1:p.Asn616Tyr
ENST00000683220.1:c.1873A>T	ENSP00000507151.1:p.Asn625Tyr
ENST00000683329.1:n.2646A>T
ENST00000683346.1:c.*1718A>T	ENSP00000507458.1:n.*1718A>T
ENST00000683459.1:n.2430A>T
ENST00000683590.1:c.1843A>T	ENSP00000506820.1:p.Asn615Tyr
ENST00000683623.1:c.1843A>T	ENSP00000507702.1:p.Asn615Tyr
ENST00000683645.1:n.2394A>T
ENST00000683694.1:n.594A>T
ENST00000683796.1:c.*1715A>T	ENSP00000508221.1:n.*1715A>T
ENST00000683802.1:n.4768A>T
ENST00000683833.1:c.1834A>T	ENSP00000506852.1:p.Asn612Tyr
ENST00000683934.1:c.1729A>T
ENST00000683989.1:c.1843A>T	ENSP00000507510.1:p.Asn615Tyr
ENST00000683994.1:c.1843A>T	ENSP00000507181.1:p.Asn615Tyr
ENST00000684290.1:c.1843A>T	ENSP00000507243.1:p.Asn615Tyr
ENST00000684306.1:c.*1756A>T	ENSP00000508384.1:n.*1756A>T
ENST00000684341.1:n.1863A>T
ENST00000684383.1:c.*1481A>T	ENSP00000506863.1:n.*1481A>T
ENST00000684482.1:c.4312A>T
ENST00000684619.1:c.*1715A>T	ENSP00000508088.1:n.*1715A>T
ENST00000684743.1:n.2874A>T
ENST00000260665.12:c.1843A>T MANE Select	ENSP00000260665.7:p.Asn615Tyr
ENST00000260665.11:c.1843A>T	ENSP00000260665.7:p.Asn615Tyr
NM_133259.3:c.1843A>T	NP_573566.2:p.Asn615Tyr
XM_006711915.2:c.1765A>T	XP_006711978.1:p.Asn589Tyr
XM_006711916.2:c.1843A>T	XP_006711979.1:p.Asn615Tyr
XM_011532473.1:c.1843A>T	XP_011530775.1:p.Asn615Tyr
XM_011532474.1:c.1843A>T	XP_011530776.1:p.Asn615Tyr
XM_006711916.3:c.1843A>T	XP_006711979.1:p.Asn615Tyr
XM_017003117.1:c.1765A>T	XP_016858606.1:p.Asn589Tyr
XR_002958896.1:n.1885A>T
NM_133259.4:c.1843A>T MANE Select	NP_573566.2:p.Asn615Tyr