Canonical Allele Identifier: CA425908245

Gene: LRPPRC

Linked Data

• MyVariant Identifiers: chr2:g.44132898G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43905759G>C , CM000664.2:g.43905759G>C	GRCh38
NC_000002.11:g.44132898G>C , CM000664.1:g.44132898G>C	GRCh37
NC_000002.10:g.43986402G>C	NCBI36
NG_008247.1:g.95247C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000472420.6:n.376C>G
ENST00000681993.1:n.849C>G
ENST00000682295.1:c.452C>G	ENSP00000507499.1:n.452C>G
ENST00000682303.1:c.*3083C>G	ENSP00000508325.1:n.*3083C>G
ENST00000682308.1:c.3297C>G	ENSP00000507056.1:p.Gly1099=
ENST00000682480.1:c.3315C>G	ENSP00000508344.1:p.Gly1105=
ENST00000682546.1:c.3294C>G	ENSP00000508188.1:p.Gly1098=
ENST00000682585.1:c.3297C>G	ENSP00000506885.1:p.Gly1099=
ENST00000682595.1:n.3881C>G
ENST00000682607.1:c.1715C>G
ENST00000682612.1:c.149C>G
ENST00000682779.1:c.3288C>G	ENSP00000507947.1:p.Gly1096=
ENST00000682845.1:n.2399C>G
ENST00000682885.1:c.3252C>G	ENSP00000508036.1:p.Gly1084=
ENST00000682933.1:n.3371C>G
ENST00000683002.1:c.149C>G
ENST00000683072.1:n.3881C>G
ENST00000683080.1:n.916C>G
ENST00000683125.1:c.3405C>G	ENSP00000507939.1:p.Gly1135=
ENST00000683213.1:c.3300C>G	ENSP00000507751.1:p.Gly1100=
ENST00000683220.1:c.3327C>G	ENSP00000507151.1:p.Gly1109=
ENST00000683329.1:n.4100C>G
ENST00000683346.1:c.*3172C>G	ENSP00000507458.1:n.*3172C>G
ENST00000683409.1:n.1904C>G
ENST00000683459.1:n.3884C>G
ENST00000683528.1:c.149C>G
ENST00000683590.1:c.3045C>G	ENSP00000506820.1:p.Gly1015=
ENST00000683623.1:c.3204C>G	ENSP00000507702.1:p.Gly1068=
ENST00000683645.1:n.3848C>G
ENST00000683796.1:c.*3169C>G	ENSP00000508221.1:n.*3169C>G
ENST00000683802.1:n.6222C>G
ENST00000683833.1:c.3288C>G	ENSP00000506852.1:p.Gly1096=
ENST00000683994.1:c.3297C>G	ENSP00000507181.1:p.Gly1099=
ENST00000684290.1:c.*833C>G	ENSP00000507243.1:n.*833C>G
ENST00000684306.1:c.*3210C>G	ENSP00000508384.1:n.*3210C>G
ENST00000684341.1:n.3317C>G
ENST00000684383.1:c.*2935C>G	ENSP00000506863.1:n.*2935C>G
ENST00000684418.1:n.4478C>G
ENST00000684454.1:n.2647C>G
ENST00000684619.1:c.*3169C>G	ENSP00000508088.1:n.*3169C>G
ENST00000684743.1:n.4328C>G
ENST00000260665.12:c.3297C>G MANE Select	ENSP00000260665.7:p.Gly1099=
ENST00000260665.11:c.3297C>G	ENSP00000260665.7:p.Gly1099=
NM_133259.3:c.3297C>G	NP_573566.2:p.Gly1099=
XM_006711915.2:c.3219C>G	XP_006711978.1:p.Gly1073=
XM_011532473.1:c.3297C>G	XP_011530775.1:p.Gly1099=
XM_011532474.1:c.3297C>G	XP_011530776.1:p.Gly1099=
XM_017003117.1:c.3219C>G	XP_016858606.1:p.Gly1073=
XR_002958896.1:n.3339C>G
NM_133259.4:c.3297C>G MANE Select	NP_573566.2:p.Gly1099=