Canonical Allele Identifier: CA346668182

Gene: LRPPRC

Linked Data

• MyVariant Identifiers: chr2:g.44145232G>T (hg19) ; chr2:g.43918093G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43918093G>T , CM000664.2:g.43918093G>T	GRCh38
NC_000002.11:g.44145232G>T , CM000664.1:g.44145232G>T	GRCh37
NC_000002.10:g.43998736G>T	NCBI36
NG_008247.1:g.82913C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681993.1:n.632C>A
ENST00000682295.1:c.303+163C>A	ENSP00000507499.1:n.303+163C>A
ENST00000682303.1:c.*2866C>A	ENSP00000508325.1:n.*2866C>A
ENST00000682308.1:c.3080C>A	ENSP00000507056.1:p.Ser1027Ter
ENST00000682480.1:c.3098C>A	ENSP00000508344.1:p.Ser1033Ter
ENST00000682546.1:c.3077C>A	ENSP00000508188.1:p.Ser1026Ter
ENST00000682585.1:c.3080C>A	ENSP00000506885.1:p.Ser1027Ter
ENST00000682595.1:n.3664C>A
ENST00000682607.1:c.1498C>A
ENST00000682779.1:c.3071C>A	ENSP00000507947.1:p.Ser1024Ter
ENST00000682845.1:n.2182C>A
ENST00000682885.1:c.3035C>A	ENSP00000508036.1:p.Ser1012Ter
ENST00000682933.1:n.3154C>A
ENST00000683072.1:n.3664C>A
ENST00000683080.1:n.699C>A
ENST00000683125.1:c.3188C>A	ENSP00000507939.1:p.Ser1063Ter
ENST00000683213.1:c.3083C>A	ENSP00000507751.1:p.Ser1028Ter
ENST00000683220.1:c.3110C>A	ENSP00000507151.1:p.Ser1037Ter
ENST00000683329.1:n.3883C>A
ENST00000683346.1:c.*2955C>A	ENSP00000507458.1:n.*2955C>A
ENST00000683409.1:n.1687C>A
ENST00000683459.1:n.3667C>A
ENST00000683590.1:c.2897-5535C>A	ENSP00000506820.1:n.2897-5535C>A
ENST00000683623.1:c.2987C>A	ENSP00000507702.1:p.Ser996Ter
ENST00000683645.1:n.3631C>A
ENST00000683796.1:c.*2952C>A	ENSP00000508221.1:n.*2952C>A
ENST00000683802.1:n.6005C>A
ENST00000683833.1:c.3071C>A	ENSP00000506852.1:p.Ser1024Ter
ENST00000683994.1:c.3080C>A	ENSP00000507181.1:p.Ser1027Ter
ENST00000684290.1:c.*616C>A	ENSP00000507243.1:n.*616C>A
ENST00000684306.1:c.*2993C>A	ENSP00000508384.1:n.*2993C>A
ENST00000684341.1:n.3100C>A
ENST00000684383.1:c.*2718C>A	ENSP00000506863.1:n.*2718C>A
ENST00000684619.1:c.*2952C>A	ENSP00000508088.1:n.*2952C>A
ENST00000684705.1:n.201C>A
ENST00000684743.1:n.4111C>A
ENST00000260665.12:c.3080C>A MANE Select	ENSP00000260665.7:p.Ser1027Ter
ENST00000260665.11:c.3080C>A	ENSP00000260665.7:p.Ser1027Ter
NM_133259.3:c.3080C>A	NP_573566.2:p.Ser1027Ter
XM_006711915.2:c.3002C>A	XP_006711978.1:p.Ser1001Ter
XM_006711916.2:c.3080C>A	XP_006711979.1:p.Ser1027Ter
XM_011532473.1:c.3080C>A	XP_011530775.1:p.Ser1027Ter
XM_011532474.1:c.3080C>A	XP_011530776.1:p.Ser1027Ter
XM_006711916.3:c.3080C>A	XP_006711979.1:p.Ser1027Ter
XM_017003117.1:c.3002C>A	XP_016858606.1:p.Ser1001Ter
XR_002958896.1:n.3122C>A
NM_133259.4:c.3080C>A MANE Select	NP_573566.2:p.Ser1027Ter