Canonical Allele Identifier: CA425908508

Gene: LRPPRC

Linked Data

• MyVariant Identifiers: chr2:g.44145228G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43918089G>C , CM000664.2:g.43918089G>C	GRCh38
NC_000002.11:g.44145228G>C , CM000664.1:g.44145228G>C	GRCh37
NC_000002.10:g.43998732G>C	NCBI36
NG_008247.1:g.82917C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681993.1:n.636C>G
ENST00000682295.1:c.303+167C>G	ENSP00000507499.1:n.303+167C>G
ENST00000682303.1:c.*2870C>G	ENSP00000508325.1:n.*2870C>G
ENST00000682308.1:c.3084C>G	ENSP00000507056.1:p.Ala1028=
ENST00000682480.1:c.3102C>G	ENSP00000508344.1:p.Ala1034=
ENST00000682546.1:c.3081C>G	ENSP00000508188.1:p.Ala1027=
ENST00000682585.1:c.3084C>G	ENSP00000506885.1:p.Ala1028=
ENST00000682595.1:n.3668C>G
ENST00000682607.1:c.1502C>G
ENST00000682779.1:c.3075C>G	ENSP00000507947.1:p.Ala1025=
ENST00000682845.1:n.2186C>G
ENST00000682885.1:c.3039C>G	ENSP00000508036.1:p.Ala1013=
ENST00000682933.1:n.3158C>G
ENST00000683072.1:n.3668C>G
ENST00000683080.1:n.703C>G
ENST00000683125.1:c.3192C>G	ENSP00000507939.1:p.Ala1064=
ENST00000683213.1:c.3087C>G	ENSP00000507751.1:p.Ala1029=
ENST00000683220.1:c.3114C>G	ENSP00000507151.1:p.Ala1038=
ENST00000683329.1:n.3887C>G
ENST00000683346.1:c.*2959C>G	ENSP00000507458.1:n.*2959C>G
ENST00000683409.1:n.1691C>G
ENST00000683459.1:n.3671C>G
ENST00000683590.1:c.2897-5531C>G	ENSP00000506820.1:n.2897-5531C>G
ENST00000683623.1:c.2991C>G	ENSP00000507702.1:p.Ala997=
ENST00000683645.1:n.3635C>G
ENST00000683796.1:c.*2956C>G	ENSP00000508221.1:n.*2956C>G
ENST00000683802.1:n.6009C>G
ENST00000683833.1:c.3075C>G	ENSP00000506852.1:p.Ala1025=
ENST00000683994.1:c.3084C>G	ENSP00000507181.1:p.Ala1028=
ENST00000684290.1:c.*620C>G	ENSP00000507243.1:n.*620C>G
ENST00000684306.1:c.*2997C>G	ENSP00000508384.1:n.*2997C>G
ENST00000684341.1:n.3104C>G
ENST00000684383.1:c.*2722C>G	ENSP00000506863.1:n.*2722C>G
ENST00000684619.1:c.*2956C>G	ENSP00000508088.1:n.*2956C>G
ENST00000684705.1:n.205C>G
ENST00000684743.1:n.4115C>G
ENST00000260665.12:c.3084C>G MANE Select	ENSP00000260665.7:p.Ala1028=
ENST00000260665.11:c.3084C>G	ENSP00000260665.7:p.Ala1028=
NM_133259.3:c.3084C>G	NP_573566.2:p.Ala1028=
XM_006711915.2:c.3006C>G	XP_006711978.1:p.Ala1002=
XM_006711916.2:c.3084C>G	XP_006711979.1:p.Ala1028=
XM_011532473.1:c.3084C>G	XP_011530775.1:p.Ala1028=
XM_011532474.1:c.3084C>G	XP_011530776.1:p.Ala1028=
XM_006711916.3:c.3084C>G	XP_006711979.1:p.Ala1028=
XM_017003117.1:c.3006C>G	XP_016858606.1:p.Ala1002=
XR_002958896.1:n.3126C>G
NM_133259.4:c.3084C>G MANE Select	NP_573566.2:p.Ala1028=