Canonical Allele Identifier: CA2493981115
Gene: LRPPRC HGNC NCBI

Linked Data

dbSNP Id: rs1671037448

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43905424_43905430dup , CM000664.2:g.43905424_43905430dup GRCh38
NC_000002.11:g.44132563_44132569dup , CM000664.1:g.44132563_44132569dup GRCh37
NC_000002.10:g.43986067_43986073dup NCBI36
NG_008247.1:g.95577_95583dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000472420.6:n.443+263_443+269dup
ENST00000681993.1:n.916+263_916+269dup
ENST00000682303.1:c.*3150+263_*3150+269dup ENSP00000508325.1:n.*3150+263_*3150+269dup
ENST00000682308.1:c.3364+263_3364+269dup ENSP00000507056.1:n.3364+263_3364+269dup
ENST00000682480.1:c.3382+263_3382+269dup ENSP00000508344.1:n.3382+263_3382+269dup
ENST00000682546.1:c.3361+263_3361+269dup ENSP00000508188.1:n.3361+263_3361+269dup
ENST00000682585.1:c.3364+263_3364+269dup ENSP00000506885.1:n.3364+263_3364+269dup
ENST00000682595.1:n.3948+263_3948+269dup
ENST00000682607.1:c.1782+263_1782+269dup
ENST00000682612.1:c.216+263_216+269dup
ENST00000682779.1:c.3355+263_3355+269dup ENSP00000507947.1:n.3355+263_3355+269dup
ENST00000682845.1:n.2466+263_2466+269dup
ENST00000682885.1:c.3319+263_3319+269dup ENSP00000508036.1:n.3319+263_3319+269dup
ENST00000682933.1:n.3438+263_3438+269dup
ENST00000683002.1:c.216+263_216+269dup
ENST00000683072.1:n.3948+263_3948+269dup
ENST00000683080.1:n.983+263_983+269dup
ENST00000683125.1:c.3472+263_3472+269dup ENSP00000507939.1:n.3472+263_3472+269dup
ENST00000683213.1:c.3367+263_3367+269dup ENSP00000507751.1:n.3367+263_3367+269dup
ENST00000683220.1:c.3394+263_3394+269dup ENSP00000507151.1:n.3394+263_3394+269dup
ENST00000683329.1:n.4167+263_4167+269dup
ENST00000683346.1:c.*3239+263_*3239+269dup ENSP00000507458.1:n.*3239+263_*3239+269dup
ENST00000683409.1:n.1971+263_1971+269dup
ENST00000683459.1:n.3951+263_3951+269dup
ENST00000683528.1:c.216+263_216+269dup
ENST00000683590.1:c.3112+263_3112+269dup ENSP00000506820.1:n.3112+263_3112+269dup
ENST00000683623.1:c.3271+263_3271+269dup ENSP00000507702.1:n.3271+263_3271+269dup
ENST00000683645.1:n.3915+263_3915+269dup
ENST00000683796.1:c.*3236+263_*3236+269dup ENSP00000508221.1:n.*3236+263_*3236+269dup
ENST00000683802.1:n.6289+263_6289+269dup
ENST00000683833.1:c.3355+263_3355+269dup ENSP00000506852.1:n.3355+263_3355+269dup
ENST00000683994.1:c.3364+263_3364+269dup ENSP00000507181.1:n.3364+263_3364+269dup
ENST00000684290.1:c.*900+263_*900+269dup ENSP00000507243.1:n.*900+263_*900+269dup
ENST00000684306.1:c.*3277+263_*3277+269dup ENSP00000508384.1:n.*3277+263_*3277+269dup
ENST00000684341.1:n.3384+263_3384+269dup
ENST00000684383.1:c.*3002+263_*3002+269dup ENSP00000506863.1:n.*3002+263_*3002+269dup
ENST00000684418.1:n.4545+263_4545+269dup
ENST00000684454.1:n.2714+263_2714+269dup
ENST00000684619.1:c.*3236+263_*3236+269dup ENSP00000508088.1:n.*3236+263_*3236+269dup
ENST00000684743.1:n.4395+263_4395+269dup
ENST00000260665.12:c.3364+263_3364+269dup MANE Select ENSP00000260665.7:n.3364+263_3364+269dup
ENST00000260665.11:c.3364+263_3364+269dup ENSP00000260665.7:n.3364+263_3364+269dup
NM_133259.3:c.3364+263_3364+269dup NP_573566.2:n.3364+263_3364+269dup
XM_006711915.2:c.3286+263_3286+269dup XP_006711978.1:n.3286+263_3286+269dup
XM_011532473.1:c.3364+263_3364+269dup XP_011530775.1:n.3364+263_3364+269dup
XM_011532474.1:c.3364+263_3364+269dup XP_011530776.1:n.3364+263_3364+269dup
XM_017003117.1:c.3286+263_3286+269dup XP_016858606.1:n.3286+263_3286+269dup
XR_002958896.1:n.3406+263_3406+269dup
NM_133259.4:c.3364+263_3364+269dup MANE Select NP_573566.2:n.3364+263_3364+269dup