Canonical Allele Identifier: CA346668351

Gene: LRPPRC

Linked Data

• MyVariant Identifiers: chr2:g.44145266A>T (hg19) ; chr2:g.43918127A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43918127A>T , CM000664.2:g.43918127A>T	GRCh38
NC_000002.11:g.44145266A>T , CM000664.1:g.44145266A>T	GRCh37
NC_000002.10:g.43998770A>T	NCBI36
NG_008247.1:g.82879T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681993.1:n.598T>A
ENST00000682295.1:c.303+129T>A	ENSP00000507499.1:n.303+129T>A
ENST00000682303.1:c.*2832T>A	ENSP00000508325.1:n.*2832T>A
ENST00000682308.1:c.3046T>A	ENSP00000507056.1:p.Tyr1016Asn
ENST00000682480.1:c.3064T>A	ENSP00000508344.1:p.Tyr1022Asn
ENST00000682546.1:c.3043T>A	ENSP00000508188.1:p.Tyr1015Asn
ENST00000682585.1:c.3046T>A	ENSP00000506885.1:p.Tyr1016Asn
ENST00000682595.1:n.3630T>A
ENST00000682607.1:c.1464T>A
ENST00000682779.1:c.3037T>A	ENSP00000507947.1:p.Tyr1013Asn
ENST00000682845.1:n.2148T>A
ENST00000682885.1:c.3001T>A	ENSP00000508036.1:p.Tyr1001Asn
ENST00000682933.1:n.3120T>A
ENST00000683072.1:n.3630T>A
ENST00000683080.1:n.665T>A
ENST00000683125.1:c.3154T>A	ENSP00000507939.1:p.Tyr1052Asn
ENST00000683213.1:c.3049T>A	ENSP00000507751.1:p.Tyr1017Asn
ENST00000683220.1:c.3076T>A	ENSP00000507151.1:p.Tyr1026Asn
ENST00000683329.1:n.3849T>A
ENST00000683346.1:c.*2921T>A	ENSP00000507458.1:n.*2921T>A
ENST00000683409.1:n.1653T>A
ENST00000683459.1:n.3633T>A
ENST00000683590.1:c.2897-5569T>A	ENSP00000506820.1:n.2897-5569T>A
ENST00000683623.1:c.2953T>A	ENSP00000507702.1:p.Tyr985Asn
ENST00000683645.1:n.3597T>A
ENST00000683796.1:c.*2918T>A	ENSP00000508221.1:n.*2918T>A
ENST00000683802.1:n.5971T>A
ENST00000683833.1:c.3037T>A	ENSP00000506852.1:p.Tyr1013Asn
ENST00000683994.1:c.3046T>A	ENSP00000507181.1:p.Tyr1016Asn
ENST00000684290.1:c.*582T>A	ENSP00000507243.1:n.*582T>A
ENST00000684306.1:c.*2959T>A	ENSP00000508384.1:n.*2959T>A
ENST00000684341.1:n.3066T>A
ENST00000684383.1:c.*2684T>A	ENSP00000506863.1:n.*2684T>A
ENST00000684619.1:c.*2918T>A	ENSP00000508088.1:n.*2918T>A
ENST00000684705.1:n.167T>A
ENST00000684743.1:n.4077T>A
ENST00000260665.12:c.3046T>A MANE Select	ENSP00000260665.7:p.Tyr1016Asn
ENST00000260665.11:c.3046T>A	ENSP00000260665.7:p.Tyr1016Asn
NM_133259.3:c.3046T>A	NP_573566.2:p.Tyr1016Asn
XM_006711915.2:c.2968T>A	XP_006711978.1:p.Tyr990Asn
XM_006711916.2:c.3046T>A	XP_006711979.1:p.Tyr1016Asn
XM_011532473.1:c.3046T>A	XP_011530775.1:p.Tyr1016Asn
XM_011532474.1:c.3046T>A	XP_011530776.1:p.Tyr1016Asn
XM_006711916.3:c.3046T>A	XP_006711979.1:p.Tyr1016Asn
XM_017003117.1:c.2968T>A	XP_016858606.1:p.Tyr990Asn
XR_002958896.1:n.3088T>A
NM_133259.4:c.3046T>A MANE Select	NP_573566.2:p.Tyr1016Asn