Canonical Allele Identifier: CA425910674

Gene: LRPPRC

Linked Data

• MyVariant Identifiers: chr2:g.44184577T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43957438T>G , CM000664.2:g.43957438T>G	GRCh38
NC_000002.11:g.44184577T>G , CM000664.1:g.44184577T>G	GRCh37
NC_000002.10:g.44038081T>G	NCBI36
NG_008247.1:g.43568A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409659.6:c.1596A>C	ENSP00000386562.2:p.Thr532=
ENST00000447246.2:c.1596A>C	ENSP00000403637.2:p.Thr532=
ENST00000467058.2:n.325A>C
ENST00000681959.1:n.1210A>C
ENST00000681961.1:n.1616A>C
ENST00000682104.1:c.1470A>C	ENSP00000507716.1:p.Thr490=
ENST00000682303.1:c.*1468A>C	ENSP00000508325.1:n.*1468A>C
ENST00000682308.1:c.1596A>C	ENSP00000507056.1:p.Thr532=
ENST00000682480.1:c.1596A>C	ENSP00000508344.1:p.Thr532=
ENST00000682546.1:c.1596A>C	ENSP00000508188.1:p.Thr532=
ENST00000682585.1:c.1596A>C	ENSP00000506885.1:p.Thr532=
ENST00000682595.1:n.2178A>C
ENST00000682607.1:c.14A>C
ENST00000682779.1:c.1587A>C	ENSP00000507947.1:p.Thr529=
ENST00000682885.1:c.1596A>C	ENSP00000508036.1:p.Thr532=
ENST00000682933.1:n.1670A>C
ENST00000683072.1:n.2178A>C
ENST00000683082.1:n.1614A>C
ENST00000683125.1:c.1596A>C	ENSP00000507939.1:p.Thr532=
ENST00000683213.1:c.1599A>C	ENSP00000507751.1:p.Thr533=
ENST00000683220.1:c.1596A>C	ENSP00000507151.1:p.Thr532=
ENST00000683329.1:n.2399A>C
ENST00000683346.1:c.*1471A>C	ENSP00000507458.1:n.*1471A>C
ENST00000683459.1:n.2183A>C
ENST00000683590.1:c.1596A>C	ENSP00000506820.1:p.Thr532=
ENST00000683623.1:c.1596A>C	ENSP00000507702.1:p.Thr532=
ENST00000683645.1:n.2116A>C
ENST00000683694.1:n.347A>C
ENST00000683796.1:c.*1468A>C	ENSP00000508221.1:n.*1468A>C
ENST00000683802.1:n.4521A>C
ENST00000683833.1:c.1587A>C	ENSP00000506852.1:p.Thr529=
ENST00000683934.1:c.1482A>C
ENST00000683989.1:c.1596A>C	ENSP00000507510.1:p.Thr532=
ENST00000683994.1:c.1596A>C	ENSP00000507181.1:p.Thr532=
ENST00000684290.1:c.1596A>C	ENSP00000507243.1:p.Thr532=
ENST00000684306.1:c.*1509A>C	ENSP00000508384.1:n.*1509A>C
ENST00000684341.1:n.1616A>C
ENST00000684383.1:c.*1234A>C	ENSP00000506863.1:n.*1234A>C
ENST00000684482.1:c.4065A>C
ENST00000684619.1:c.*1468A>C	ENSP00000508088.1:n.*1468A>C
ENST00000684743.1:n.2627A>C
ENST00000260665.12:c.1596A>C MANE Select	ENSP00000260665.7:p.Thr532=
ENST00000260665.11:c.1596A>C	ENSP00000260665.7:p.Thr532=
ENST00000467058.1:n.325A>C
NM_133259.3:c.1596A>C	NP_573566.2:p.Thr532=
XM_006711915.2:c.1518A>C	XP_006711978.1:p.Thr506=
XM_006711916.2:c.1596A>C	XP_006711979.1:p.Thr532=
XM_011532473.1:c.1596A>C	XP_011530775.1:p.Thr532=
XM_011532474.1:c.1596A>C	XP_011530776.1:p.Thr532=
XM_006711916.3:c.1596A>C	XP_006711979.1:p.Thr532=
XM_017003117.1:c.1518A>C	XP_016858606.1:p.Thr506=
XR_002958896.1:n.1638A>C
NM_133259.4:c.1596A>C MANE Select	NP_573566.2:p.Thr532=