Canonical Allele Identifier: CA10581495
Gene: ITPR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 235919
dbSNP Id: rs878853175

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.4815182_4815184del , CM000665.2:g.4815182_4815184del GRCh38
NC_000003.11:g.4856866_4856868del , CM000665.1:g.4856866_4856868del GRCh37
NC_000003.10:g.4831866_4831868del NCBI36
NG_016144.1:g.326835_326837del

Transcript Alleles

HGVS Amino-acid change
ENST00000302640.13:c.7842_7844del ENSP00000306253.9:n.7842_7844del
ENST00000354582.12:c.7807_7809del ENSP00000346595.8:p.Lys2603del
ENST00000443694.5:c.7786_7788del ENSP00000401671.2:p.Lys2596del
ENST00000354582.11:c.7807_7809del ENSP00000346595.8:p.Lys2603del
ENST00000357086.10:c.7687_7689del ENSP00000349597.4:p.Lys2563del
ENST00000443694.4:c.7786_7788del ENSP00000401671.2:p.Lys2596del
ENST00000456211.8:c.7642_7644del ENSP00000397885.2:p.Lys2548del
ENST00000463980.6:n.1148_1150del
ENST00000467545.6:n.1088_1090del
ENST00000478515.2:c.165_167del
ENST00000493491.6:n.1109_1111del
ENST00000544951.6:c.1720_1722del ENSP00000440564.1:p.Lys574del
ENST00000647685.1:c.82_84del ENSP00000497835.1:p.Lys28del
ENST00000647708.1:c.3730_3732del
ENST00000647717.1:n.5335_5337del
ENST00000647997.1:n.851_853del
ENST00000648016.1:c.4199_4201del
ENST00000648038.1:c.5593_5595del ENSP00000497872.1:p.Lys1865del
ENST00000648208.1:n.842_844del
ENST00000648212.1:c.4772_4774del
ENST00000648266.1:c.7804_7806del ENSP00000498014.1:p.Lys2602del
ENST00000648309.1:c.7759_7761del ENSP00000497026.1:p.Lys2587del
ENST00000648390.1:c.447-30957_447-30955del
ENST00000648431.1:c.5010_5012del
ENST00000648770.1:n.925_927del
ENST00000649015.2:c.7831_7833del MANE Select ENSP00000497605.1:p.Lys2611del
ENST00000649139.1:c.82_84del ENSP00000497226.1:p.Lys28del
ENST00000649144.1:n.2879_2881del
ENST00000649314.1:n.959_961del
ENST00000649430.1:n.370_372del
ENST00000649694.1:n.5316_5318del
ENST00000649767.1:n.1163_1165del
ENST00000649908.1:c.82_84del ENSP00000497614.1:p.Lys28del
ENST00000650074.1:n.1141_1143del
ENST00000650139.1:n.2595_2597del
ENST00000650294.1:c.7789_7791del ENSP00000498056.1:p.Lys2597del
ENST00000650552.1:n.1257_1259del
ENST00000302640.12:c.7786_7788del ENSP00000306253.8:p.Lys2596del
ENST00000354582.10:c.7831_7833del ENSP00000346595.7:p.Lys2611del
ENST00000357086.9:c.7687_7689del ENSP00000349597.4:p.Lys2563del
ENST00000443694.3:c.7786_7788del ENSP00000401671.2:p.Lys2596del
ENST00000456211.7:c.7642_7644del ENSP00000397885.2:p.Lys2548del
ENST00000463980.5:n.1133_1135del
ENST00000472205.1:n.458_460del
ENST00000478515.1:n.538_540del
ENST00000493491.5:n.1109_1111del
ENST00000544951.5:c.1720_1722del ENSP00000440564.1:p.Lys574del
NM_001099952.2:c.7687_7689del NP_001093422.2:p.Lys2563del
NM_001168272.1:c.7786_7788del NP_001161744.1:p.Lys2596del
NM_002222.5:c.7642_7644del NP_002213.5:p.Lys2548del
XM_005265109.2:c.7762_7764del XP_005265166.1:p.Lys2588del
XM_005265110.2:c.7714_7716del XP_005265167.1:p.Lys2572del
XM_006713131.2:c.7765_7767del XP_006713194.1:p.Lys2589del
XM_011533681.1:c.7834_7836del XP_011531983.1:p.Lys2612del
XM_011533682.1:c.7834_7836del XP_011531984.1:p.Lys2612del
XM_011533683.1:c.7831_7833del XP_011531985.1:p.Lys2611del
XM_011533684.1:c.7807_7809del XP_011531986.1:p.Lys2603del
XM_011533685.1:c.7801_7803del XP_011531987.1:p.Lys2601del
XM_011533686.1:c.7798_7800del XP_011531988.1:p.Lys2600del
XM_011533687.1:c.7789_7791del XP_011531989.1:p.Lys2597del
XM_011533688.1:c.7762_7764del XP_011531990.1:p.Lys2588del
XM_011533689.1:c.7723_7725del XP_011531991.1:p.Lys2575del
XM_011533690.1:c.7711_7713del XP_011531992.1:p.Lys2571del
XM_005265109.3:c.7762_7764del XP_005265166.1:p.Lys2588del
XM_005265110.3:c.7714_7716del XP_005265167.1:p.Lys2572del
XM_006713131.3:c.7765_7767del XP_006713194.1:p.Lys2589del
XM_011533682.3:c.7834_7836del XP_011531984.1:p.Lys2612del
XM_011533683.3:c.7831_7833del XP_011531985.1:p.Lys2611del
XM_011533684.2:c.7807_7809del XP_011531986.1:p.Lys2603del
XM_011533685.2:c.7801_7803del XP_011531987.1:p.Lys2601del
XM_011533686.2:c.7798_7800del XP_011531988.1:p.Lys2600del
XM_011533687.2:c.7789_7791del XP_011531989.1:p.Lys2597del
XM_011533688.2:c.7762_7764del XP_011531990.1:p.Lys2588del
XM_011533690.2:c.7711_7713del XP_011531992.1:p.Lys2571del
XM_017006357.2:c.7708_7710del XP_016861846.1:p.Lys2570del
NM_001099952.3:c.7687_7689del NP_001093422.2:p.Lys2563del
NM_002222.6:c.7642_7644del NP_002213.5:p.Lys2548del
NM_001099952.4:c.7687_7689del NP_001093422.2:p.Lys2563del
NM_001168272.2:c.7786_7788del NP_001161744.1:p.Lys2596del
NM_001378452.1:c.7831_7833del MANE Select NP_001365381.1:p.Lys2611del
NM_002222.7:c.7642_7644del NP_002213.5:p.Lys2548del