Canonical Allele Identifier: CA425908220

Gene: LRPPRC

Linked Data

• MyVariant Identifiers: chr2:g.44132877G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43905738G>T , CM000664.2:g.43905738G>T	GRCh38
NC_000002.11:g.44132877G>T , CM000664.1:g.44132877G>T	GRCh37
NC_000002.10:g.43986381G>T	NCBI36
NG_008247.1:g.95268C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000472420.6:n.397C>A
ENST00000681993.1:n.870C>A
ENST00000682295.1:c.473C>A	ENSP00000507499.1:n.473C>A
ENST00000682303.1:c.*3104C>A	ENSP00000508325.1:n.*3104C>A
ENST00000682308.1:c.3318C>A	ENSP00000507056.1:p.Ala1106=
ENST00000682480.1:c.3336C>A	ENSP00000508344.1:p.Ala1112=
ENST00000682546.1:c.3315C>A	ENSP00000508188.1:p.Ala1105=
ENST00000682585.1:c.3318C>A	ENSP00000506885.1:p.Ala1106=
ENST00000682595.1:n.3902C>A
ENST00000682607.1:c.1736C>A
ENST00000682612.1:c.170C>A
ENST00000682779.1:c.3309C>A	ENSP00000507947.1:p.Ala1103=
ENST00000682845.1:n.2420C>A
ENST00000682885.1:c.3273C>A	ENSP00000508036.1:p.Ala1091=
ENST00000682933.1:n.3392C>A
ENST00000683002.1:c.170C>A
ENST00000683072.1:n.3902C>A
ENST00000683080.1:n.937C>A
ENST00000683125.1:c.3426C>A	ENSP00000507939.1:p.Ala1142=
ENST00000683213.1:c.3321C>A	ENSP00000507751.1:p.Ala1107=
ENST00000683220.1:c.3348C>A	ENSP00000507151.1:p.Ala1116=
ENST00000683329.1:n.4121C>A
ENST00000683346.1:c.*3193C>A	ENSP00000507458.1:n.*3193C>A
ENST00000683409.1:n.1925C>A
ENST00000683459.1:n.3905C>A
ENST00000683528.1:c.170C>A
ENST00000683590.1:c.3066C>A	ENSP00000506820.1:p.Ala1022=
ENST00000683623.1:c.3225C>A	ENSP00000507702.1:p.Ala1075=
ENST00000683645.1:n.3869C>A
ENST00000683796.1:c.*3190C>A	ENSP00000508221.1:n.*3190C>A
ENST00000683802.1:n.6243C>A
ENST00000683833.1:c.3309C>A	ENSP00000506852.1:p.Ala1103=
ENST00000683994.1:c.3318C>A	ENSP00000507181.1:p.Ala1106=
ENST00000684290.1:c.*854C>A	ENSP00000507243.1:n.*854C>A
ENST00000684306.1:c.*3231C>A	ENSP00000508384.1:n.*3231C>A
ENST00000684341.1:n.3338C>A
ENST00000684383.1:c.*2956C>A	ENSP00000506863.1:n.*2956C>A
ENST00000684418.1:n.4499C>A
ENST00000684454.1:n.2668C>A
ENST00000684619.1:c.*3190C>A	ENSP00000508088.1:n.*3190C>A
ENST00000684743.1:n.4349C>A
ENST00000260665.12:c.3318C>A MANE Select	ENSP00000260665.7:p.Ala1106=
ENST00000260665.11:c.3318C>A	ENSP00000260665.7:p.Ala1106=
NM_133259.3:c.3318C>A	NP_573566.2:p.Ala1106=
XM_006711915.2:c.3240C>A	XP_006711978.1:p.Ala1080=
XM_011532473.1:c.3318C>A	XP_011530775.1:p.Ala1106=
XM_011532474.1:c.3318C>A	XP_011530776.1:p.Ala1106=
XM_017003117.1:c.3240C>A	XP_016858606.1:p.Ala1080=
XR_002958896.1:n.3360C>A
NM_133259.4:c.3318C>A MANE Select	NP_573566.2:p.Ala1106=