Canonical Allele Identifier: CA913189775

Gene: LRPPRC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43995951T>C , CM000664.2:g.43995951T>C	GRCh38
NC_000002.11:g.44223090T>C , CM000664.1:g.44223090T>C	GRCh37
NC_000002.10:g.44076594T>C	NCBI36
NG_008247.1:g.5055A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409659.6:c.-4A>G	ENSP00000386562.2:n.-4A>G
ENST00000409946.6:c.-4A>G	ENSP00000386234.1:n.-4A>G
ENST00000447246.2:c.-4A>G	ENSP00000403637.2:n.-4A>G
ENST00000681961.1:n.17A>G
ENST00000682104.1:c.23+189A>G	ENSP00000507716.1:n.23+189A>G
ENST00000682303.1:c.-4A>G	ENSP00000508325.1:n.-4A>G
ENST00000682308.1:c.-4A>G	ENSP00000507056.1:n.-4A>G
ENST00000682480.1:c.-4A>G	ENSP00000508344.1:n.-4A>G
ENST00000682546.1:c.-4A>G	ENSP00000508188.1:n.-4A>G
ENST00000682585.1:c.-4A>G	ENSP00000506885.1:n.-4A>G
ENST00000682595.1:n.12A>G
ENST00000682779.1:c.-4A>G	ENSP00000507947.1:n.-4A>G
ENST00000682885.1:c.-4A>G	ENSP00000508036.1:n.-4A>G
ENST00000683072.1:n.12A>G
ENST00000683082.1:n.15A>G
ENST00000683125.1:c.-4A>G	ENSP00000507939.1:n.-4A>G
ENST00000683213.1:c.-4A>G	ENSP00000507751.1:n.-4A>G
ENST00000683220.1:c.-4A>G	ENSP00000507151.1:n.-4A>G
ENST00000683329.1:n.36A>G
ENST00000683346.1:c.-4A>G	ENSP00000507458.1:n.-4A>G
ENST00000683459.1:n.17A>G
ENST00000683590.1:c.-4A>G	ENSP00000506820.1:n.-4A>G
ENST00000683623.1:c.-4A>G	ENSP00000507702.1:n.-4A>G
ENST00000683796.1:c.-4A>G	ENSP00000508221.1:n.-4A>G
ENST00000683833.1:c.-4A>G	ENSP00000506852.1:n.-4A>G
ENST00000683989.1:c.-4A>G	ENSP00000507510.1:n.-4A>G
ENST00000683994.1:c.-4A>G	ENSP00000507181.1:n.-4A>G
ENST00000684290.1:c.-4A>G	ENSP00000507243.1:n.-4A>G
ENST00000684306.1:c.-4A>G	ENSP00000508384.1:n.-4A>G
ENST00000684329.1:n.39A>G
ENST00000684341.1:n.17A>G
ENST00000684383.1:c.-4A>G	ENSP00000506863.1:n.-4A>G
ENST00000684619.1:c.-4A>G	ENSP00000508088.1:n.-4A>G
ENST00000684691.1:n.39A>G
ENST00000260665.12:c.-4A>G MANE Select	ENSP00000260665.7:n.-4A>G
ENST00000260665.11:c.-4A>G	ENSP00000260665.7:n.-4A>G
ENST00000409659.5:c.-4A>G	ENSP00000386562.1:n.-4A>G
ENST00000409946.5:c.-4A>G	ENSP00000386234.1:n.-4A>G
ENST00000447246.1:c.-107A>G	ENSP00000403637.1:n.-107A>G
NM_133259.3:c.-4A>G	NP_573566.2:n.-4A>G
XM_006711915.2:c.-107A>G	XP_006711978.1:n.-107A>G
XM_006711916.2:c.-4A>G	XP_006711979.1:n.-4A>G
XM_011532473.1:c.-4A>G	XP_011530775.1:n.-4A>G
XM_011532474.1:c.-4A>G	XP_011530776.1:n.-4A>G
XM_006711916.3:c.-4A>G	XP_006711979.1:n.-4A>G
XM_017003117.1:c.-107A>G	XP_016858606.1:n.-107A>G
XR_002958896.1:n.39A>G
NM_133259.4:c.-4A>G MANE Select	NP_573566.2:n.-4A>G