Canonical Allele Identifier: CA425908456

Gene: LRPPRC

Linked Data

• MyVariant Identifiers: chr2:g.44145165T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43918026T>C , CM000664.2:g.43918026T>C	GRCh38
NC_000002.11:g.44145165T>C , CM000664.1:g.44145165T>C	GRCh37
NC_000002.10:g.43998669T>C	NCBI36
NG_008247.1:g.82980A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681993.1:n.699A>G
ENST00000682295.1:c.303+230A>G	ENSP00000507499.1:n.303+230A>G
ENST00000682303.1:c.*2933A>G	ENSP00000508325.1:n.*2933A>G
ENST00000682308.1:c.3147A>G	ENSP00000507056.1:p.Lys1049=
ENST00000682480.1:c.3165A>G	ENSP00000508344.1:p.Lys1055=
ENST00000682546.1:c.3144A>G	ENSP00000508188.1:p.Lys1048=
ENST00000682585.1:c.3147A>G	ENSP00000506885.1:p.Lys1049=
ENST00000682595.1:n.3731A>G
ENST00000682607.1:c.1565A>G
ENST00000682779.1:c.3138A>G	ENSP00000507947.1:p.Lys1046=
ENST00000682845.1:n.2249A>G
ENST00000682885.1:c.3102A>G	ENSP00000508036.1:p.Lys1034=
ENST00000682933.1:n.3221A>G
ENST00000683072.1:n.3731A>G
ENST00000683080.1:n.766A>G
ENST00000683125.1:c.3255A>G	ENSP00000507939.1:p.Lys1085=
ENST00000683213.1:c.3150A>G	ENSP00000507751.1:p.Lys1050=
ENST00000683220.1:c.3177A>G	ENSP00000507151.1:p.Lys1059=
ENST00000683329.1:n.3950A>G
ENST00000683346.1:c.*3022A>G	ENSP00000507458.1:n.*3022A>G
ENST00000683409.1:n.1754A>G
ENST00000683459.1:n.3734A>G
ENST00000683590.1:c.2897-5468A>G	ENSP00000506820.1:n.2897-5468A>G
ENST00000683623.1:c.3054A>G	ENSP00000507702.1:p.Lys1018=
ENST00000683645.1:n.3698A>G
ENST00000683796.1:c.*3019A>G	ENSP00000508221.1:n.*3019A>G
ENST00000683802.1:n.6072A>G
ENST00000683833.1:c.3138A>G	ENSP00000506852.1:p.Lys1046=
ENST00000683994.1:c.3147A>G	ENSP00000507181.1:p.Lys1049=
ENST00000684290.1:c.*683A>G	ENSP00000507243.1:n.*683A>G
ENST00000684306.1:c.*3060A>G	ENSP00000508384.1:n.*3060A>G
ENST00000684341.1:n.3167A>G
ENST00000684383.1:c.*2785A>G	ENSP00000506863.1:n.*2785A>G
ENST00000684619.1:c.*3019A>G	ENSP00000508088.1:n.*3019A>G
ENST00000684705.1:n.268A>G
ENST00000684743.1:n.4178A>G
ENST00000260665.12:c.3147A>G MANE Select	ENSP00000260665.7:p.Lys1049=
ENST00000260665.11:c.3147A>G	ENSP00000260665.7:p.Lys1049=
NM_133259.3:c.3147A>G	NP_573566.2:p.Lys1049=
XM_006711915.2:c.3069A>G	XP_006711978.1:p.Lys1023=
XM_006711916.2:c.3147A>G	XP_006711979.1:p.Lys1049=
XM_011532473.1:c.3147A>G	XP_011530775.1:p.Lys1049=
XM_011532474.1:c.3147A>G	XP_011530776.1:p.Lys1049=
XM_006711916.3:c.3147A>G	XP_006711979.1:p.Lys1049=
XM_017003117.1:c.3069A>G	XP_016858606.1:p.Lys1023=
XR_002958896.1:n.3189A>G
NM_133259.4:c.3147A>G MANE Select	NP_573566.2:p.Lys1049=