Canonical Allele Identifier: CA425909304

Gene: LRPPRC

Linked Data

• MyVariant Identifiers: chr2:g.44126469G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43899330G>A , CM000664.2:g.43899330G>A	GRCh38
NC_000002.11:g.44126469G>A , CM000664.1:g.44126469G>A	GRCh37
NC_000002.10:g.43979973G>A	NCBI36
NG_008247.1:g.101676C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000419884.6:c.145C>T
ENST00000472420.6:n.793C>T
ENST00000483489.2:n.145C>T
ENST00000681993.1:n.1266C>T
ENST00000682303.1:c.*3500C>T	ENSP00000508325.1:n.*3500C>T
ENST00000682308.1:c.3714C>T	ENSP00000507056.1:p.Ser1238=
ENST00000682434.1:n.1265C>T
ENST00000682480.1:c.3732C>T	ENSP00000508344.1:p.Ser1244=
ENST00000682546.1:c.3711C>T	ENSP00000508188.1:p.Ser1237=
ENST00000682585.1:c.3714C>T	ENSP00000506885.1:p.Ser1238=
ENST00000682595.1:n.4298C>T
ENST00000682607.1:c.2132C>T
ENST00000682612.1:c.566C>T
ENST00000682779.1:c.3705C>T	ENSP00000507947.1:p.Ser1235=
ENST00000682845.1:n.2816C>T
ENST00000682885.1:c.3669C>T	ENSP00000508036.1:p.Ser1223=
ENST00000682933.1:n.3788C>T
ENST00000683002.1:c.566C>T
ENST00000683072.1:n.4298C>T
ENST00000683080.1:n.1333C>T
ENST00000683125.1:c.3822C>T	ENSP00000507939.1:p.Ser1274=
ENST00000683213.1:c.3717C>T	ENSP00000507751.1:p.Ser1239=
ENST00000683220.1:c.3744C>T	ENSP00000507151.1:p.Ser1248=
ENST00000683329.1:n.4517C>T
ENST00000683346.1:c.*3589C>T	ENSP00000507458.1:n.*3589C>T
ENST00000683409.1:n.2321C>T
ENST00000683459.1:n.4301C>T
ENST00000683528.1:c.642C>T
ENST00000683590.1:c.3462C>T	ENSP00000506820.1:p.Ser1154=
ENST00000683623.1:c.3621C>T	ENSP00000507702.1:p.Ser1207=
ENST00000683645.1:n.4265C>T
ENST00000683796.1:c.*3586C>T	ENSP00000508221.1:n.*3586C>T
ENST00000683802.1:n.6639C>T
ENST00000683833.1:c.3705C>T	ENSP00000506852.1:p.Ser1235=
ENST00000683994.1:c.3714C>T	ENSP00000507181.1:p.Ser1238=
ENST00000684290.1:c.*1250C>T	ENSP00000507243.1:n.*1250C>T
ENST00000684306.1:c.*3627C>T	ENSP00000508384.1:n.*3627C>T
ENST00000684341.1:n.3734C>T
ENST00000684383.1:c.*3352C>T	ENSP00000506863.1:n.*3352C>T
ENST00000684418.1:n.4895C>T
ENST00000684433.1:n.98C>T
ENST00000684454.1:n.3064C>T
ENST00000684619.1:c.*3586C>T	ENSP00000508088.1:n.*3586C>T
ENST00000684743.1:n.6459C>T
ENST00000260665.12:c.3714C>T MANE Select	ENSP00000260665.7:p.Ser1238=
ENST00000260665.11:c.3714C>T	ENSP00000260665.7:p.Ser1238=
ENST00000463456.5:n.2757C>T
ENST00000472420.5:n.111C>T
ENST00000483489.1:n.188C>T
NM_133259.3:c.3714C>T	NP_573566.2:p.Ser1238=
XM_006711915.2:c.3636C>T	XP_006711978.1:p.Ser1212=
XM_011532473.1:c.3714C>T	XP_011530775.1:p.Ser1238=
XM_011532474.1:c.3714C>T	XP_011530776.1:p.Ser1238=
XM_017003117.1:c.3636C>T	XP_016858606.1:p.Ser1212=
XR_002958896.1:n.3756C>T
NM_133259.4:c.3714C>T MANE Select	NP_573566.2:p.Ser1238=