Canonical Allele Identifier: CA346668232

Gene: LRPPRC

Linked Data

• MyVariant Identifiers: chr2:g.44145242T>C (hg19) ; chr2:g.43918103T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43918103T>C , CM000664.2:g.43918103T>C	GRCh38
NC_000002.11:g.44145242T>C , CM000664.1:g.44145242T>C	GRCh37
NC_000002.10:g.43998746T>C	NCBI36
NG_008247.1:g.82903A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681993.1:n.622A>G
ENST00000682295.1:c.303+153A>G	ENSP00000507499.1:n.303+153A>G
ENST00000682303.1:c.*2856A>G	ENSP00000508325.1:n.*2856A>G
ENST00000682308.1:c.3070A>G	ENSP00000507056.1:p.Asn1024Asp
ENST00000682480.1:c.3088A>G	ENSP00000508344.1:p.Asn1030Asp
ENST00000682546.1:c.3067A>G	ENSP00000508188.1:p.Asn1023Asp
ENST00000682585.1:c.3070A>G	ENSP00000506885.1:p.Asn1024Asp
ENST00000682595.1:n.3654A>G
ENST00000682607.1:c.1488A>G
ENST00000682779.1:c.3061A>G	ENSP00000507947.1:p.Asn1021Asp
ENST00000682845.1:n.2172A>G
ENST00000682885.1:c.3025A>G	ENSP00000508036.1:p.Asn1009Asp
ENST00000682933.1:n.3144A>G
ENST00000683072.1:n.3654A>G
ENST00000683080.1:n.689A>G
ENST00000683125.1:c.3178A>G	ENSP00000507939.1:p.Asn1060Asp
ENST00000683213.1:c.3073A>G	ENSP00000507751.1:p.Asn1025Asp
ENST00000683220.1:c.3100A>G	ENSP00000507151.1:p.Asn1034Asp
ENST00000683329.1:n.3873A>G
ENST00000683346.1:c.*2945A>G	ENSP00000507458.1:n.*2945A>G
ENST00000683409.1:n.1677A>G
ENST00000683459.1:n.3657A>G
ENST00000683590.1:c.2897-5545A>G	ENSP00000506820.1:n.2897-5545A>G
ENST00000683623.1:c.2977A>G	ENSP00000507702.1:p.Asn993Asp
ENST00000683645.1:n.3621A>G
ENST00000683796.1:c.*2942A>G	ENSP00000508221.1:n.*2942A>G
ENST00000683802.1:n.5995A>G
ENST00000683833.1:c.3061A>G	ENSP00000506852.1:p.Asn1021Asp
ENST00000683994.1:c.3070A>G	ENSP00000507181.1:p.Asn1024Asp
ENST00000684290.1:c.*606A>G	ENSP00000507243.1:n.*606A>G
ENST00000684306.1:c.*2983A>G	ENSP00000508384.1:n.*2983A>G
ENST00000684341.1:n.3090A>G
ENST00000684383.1:c.*2708A>G	ENSP00000506863.1:n.*2708A>G
ENST00000684619.1:c.*2942A>G	ENSP00000508088.1:n.*2942A>G
ENST00000684705.1:n.191A>G
ENST00000684743.1:n.4101A>G
ENST00000260665.12:c.3070A>G MANE Select	ENSP00000260665.7:p.Asn1024Asp
ENST00000260665.11:c.3070A>G	ENSP00000260665.7:p.Asn1024Asp
NM_133259.3:c.3070A>G	NP_573566.2:p.Asn1024Asp
XM_006711915.2:c.2992A>G	XP_006711978.1:p.Asn998Asp
XM_006711916.2:c.3070A>G	XP_006711979.1:p.Asn1024Asp
XM_011532473.1:c.3070A>G	XP_011530775.1:p.Asn1024Asp
XM_011532474.1:c.3070A>G	XP_011530776.1:p.Asn1024Asp
XM_006711916.3:c.3070A>G	XP_006711979.1:p.Asn1024Asp
XM_017003117.1:c.2992A>G	XP_016858606.1:p.Asn998Asp
XR_002958896.1:n.3112A>G
NM_133259.4:c.3070A>G MANE Select	NP_573566.2:p.Asn1024Asp