Canonical Allele Identifier: CA346678579

Gene: LRPPRC

Linked Data

• gnomAD v4: 2-43957439-G-C
• MyVariant Identifiers: chr2:g.44184578G>C (hg19) ; chr2:g.43957439G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43957439G>C , CM000664.2:g.43957439G>C	GRCh38
NC_000002.11:g.44184578G>C , CM000664.1:g.44184578G>C	GRCh37
NC_000002.10:g.44038082G>C	NCBI36
NG_008247.1:g.43567C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409659.6:c.1595C>G	ENSP00000386562.2:p.Thr532Arg
ENST00000447246.2:c.1595C>G	ENSP00000403637.2:p.Thr532Arg
ENST00000467058.2:n.324C>G
ENST00000681959.1:n.1209C>G
ENST00000681961.1:n.1615C>G
ENST00000682104.1:c.1469C>G	ENSP00000507716.1:p.Thr490Arg
ENST00000682303.1:c.*1467C>G	ENSP00000508325.1:n.*1467C>G
ENST00000682308.1:c.1595C>G	ENSP00000507056.1:p.Thr532Arg
ENST00000682480.1:c.1595C>G	ENSP00000508344.1:p.Thr532Arg
ENST00000682546.1:c.1595C>G	ENSP00000508188.1:p.Thr532Arg
ENST00000682585.1:c.1595C>G	ENSP00000506885.1:p.Thr532Arg
ENST00000682595.1:n.2177C>G
ENST00000682607.1:c.13C>G
ENST00000682779.1:c.1586C>G	ENSP00000507947.1:p.Thr529Arg
ENST00000682885.1:c.1595C>G	ENSP00000508036.1:p.Thr532Arg
ENST00000682933.1:n.1669C>G
ENST00000683072.1:n.2177C>G
ENST00000683082.1:n.1613C>G
ENST00000683125.1:c.1595C>G	ENSP00000507939.1:p.Thr532Arg
ENST00000683213.1:c.1598C>G	ENSP00000507751.1:p.Thr533Arg
ENST00000683220.1:c.1595C>G	ENSP00000507151.1:p.Thr532Arg
ENST00000683329.1:n.2398C>G
ENST00000683346.1:c.*1470C>G	ENSP00000507458.1:n.*1470C>G
ENST00000683459.1:n.2182C>G
ENST00000683590.1:c.1595C>G	ENSP00000506820.1:p.Thr532Arg
ENST00000683623.1:c.1595C>G	ENSP00000507702.1:p.Thr532Arg
ENST00000683645.1:n.2115C>G
ENST00000683694.1:n.346C>G
ENST00000683796.1:c.*1467C>G	ENSP00000508221.1:n.*1467C>G
ENST00000683802.1:n.4520C>G
ENST00000683833.1:c.1586C>G	ENSP00000506852.1:p.Thr529Arg
ENST00000683934.1:c.1481C>G
ENST00000683989.1:c.1595C>G	ENSP00000507510.1:p.Thr532Arg
ENST00000683994.1:c.1595C>G	ENSP00000507181.1:p.Thr532Arg
ENST00000684290.1:c.1595C>G	ENSP00000507243.1:p.Thr532Arg
ENST00000684306.1:c.*1508C>G	ENSP00000508384.1:n.*1508C>G
ENST00000684341.1:n.1615C>G
ENST00000684383.1:c.*1233C>G	ENSP00000506863.1:n.*1233C>G
ENST00000684482.1:c.4064C>G
ENST00000684619.1:c.*1467C>G	ENSP00000508088.1:n.*1467C>G
ENST00000684743.1:n.2626C>G
ENST00000260665.12:c.1595C>G MANE Select	ENSP00000260665.7:p.Thr532Arg
ENST00000260665.11:c.1595C>G	ENSP00000260665.7:p.Thr532Arg
ENST00000467058.1:n.324C>G
NM_133259.3:c.1595C>G	NP_573566.2:p.Thr532Arg
XM_006711915.2:c.1517C>G	XP_006711978.1:p.Thr506Arg
XM_006711916.2:c.1595C>G	XP_006711979.1:p.Thr532Arg
XM_011532473.1:c.1595C>G	XP_011530775.1:p.Thr532Arg
XM_011532474.1:c.1595C>G	XP_011530776.1:p.Thr532Arg
XM_006711916.3:c.1595C>G	XP_006711979.1:p.Thr532Arg
XM_017003117.1:c.1517C>G	XP_016858606.1:p.Thr506Arg
XR_002958896.1:n.1637C>G
NM_133259.4:c.1595C>G MANE Select	NP_573566.2:p.Thr532Arg