Canonical Allele Identifier: CA1342337419
Gene: ITPR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.4787982C= , CM000665.2:g.4787982C= GRCh38
NC_000003.11:g.4829666C= , CM000665.1:g.4829666C= GRCh37
NC_000003.10:g.4804666C= NCBI36
NG_016144.1:g.299635C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000302640.13:c.6662C= ENSP00000306253.9:n.6662C=
ENST00000354582.12:c.6627C= ENSP00000346595.8:p.Val2209=
ENST00000443694.5:c.6606C= ENSP00000401671.2:p.Val2202=
ENST00000354582.11:c.6627C= ENSP00000346595.8:p.Val2209=
ENST00000357086.10:c.6507C= ENSP00000349597.4:p.Val2169=
ENST00000443694.4:c.6606C= ENSP00000401671.2:p.Val2202=
ENST00000456211.8:c.6462C= ENSP00000397885.2:p.Val2154=
ENST00000481415.2:n.543C=
ENST00000544951.6:c.997-18121C= ENSP00000440564.1:n.997-18121C=
ENST00000647708.1:c.2550C=
ENST00000647717.1:n.4155C=
ENST00000648016.1:c.2986C=
ENST00000648038.1:c.4413C= ENSP00000497872.1:p.Val1471=
ENST00000648212.1:c.3559C=
ENST00000648266.1:c.6624C= ENSP00000498014.1:p.Val2208=
ENST00000648309.1:c.6579C= ENSP00000497026.1:p.Val2193=
ENST00000648390.1:c.447-58157C=
ENST00000648431.1:c.3953C=
ENST00000648510.1:n.485C=
ENST00000649015.2:c.6651C= MANE Select ENSP00000497605.1:p.Val2217=
ENST00000649144.1:n.1699C=
ENST00000649272.1:n.213C=
ENST00000649694.1:n.4136C=
ENST00000650294.1:c.6609C= ENSP00000498056.1:p.Val2203=
ENST00000302640.12:c.6606C= ENSP00000306253.8:p.Val2202=
ENST00000354582.10:c.6651C= ENSP00000346595.7:p.Val2217=
ENST00000357086.9:c.6507C= ENSP00000349597.4:p.Val2169=
ENST00000443694.3:c.6606C= ENSP00000401671.2:p.Val2202=
ENST00000456211.7:c.6462C= ENSP00000397885.2:p.Val2154=
ENST00000481415.1:n.543C=
ENST00000544951.5:c.997-18121C= ENSP00000440564.1:n.997-18121C=
NM_001099952.2:c.6507C= NP_001093422.2:p.Val2169=
NM_001168272.1:c.6606C= NP_001161744.1:p.Val2202=
NM_002222.5:c.6462C= NP_002213.5:p.Val2154=
XM_005265109.2:c.6582C= XP_005265166.1:p.Val2194=
XM_005265110.2:c.6534C= XP_005265167.1:p.Val2178=
XM_006713131.2:c.6585C= XP_006713194.1:p.Val2195=
XM_011533681.1:c.6654C= XP_011531983.1:p.Val2218=
XM_011533682.1:c.6654C= XP_011531984.1:p.Val2218=
XM_011533683.1:c.6651C= XP_011531985.1:p.Val2217=
XM_011533684.1:c.6627C= XP_011531986.1:p.Val2209=
XM_011533685.1:c.6621C= XP_011531987.1:p.Val2207=
XM_011533686.1:c.6618C= XP_011531988.1:p.Val2206=
XM_011533687.1:c.6609C= XP_011531989.1:p.Val2203=
XM_011533688.1:c.6582C= XP_011531990.1:p.Val2194=
XM_011533689.1:c.6543C= XP_011531991.1:p.Val2181=
XM_011533690.1:c.6654C= XP_011531992.1:p.Val2218=
XM_005265109.3:c.6582C= XP_005265166.1:p.Val2194=
XM_005265110.3:c.6534C= XP_005265167.1:p.Val2178=
XM_006713131.3:c.6585C= XP_006713194.1:p.Val2195=
XM_011533682.3:c.6654C= XP_011531984.1:p.Val2218=
XM_011533683.3:c.6651C= XP_011531985.1:p.Val2217=
XM_011533684.2:c.6627C= XP_011531986.1:p.Val2209=
XM_011533685.2:c.6621C= XP_011531987.1:p.Val2207=
XM_011533686.2:c.6618C= XP_011531988.1:p.Val2206=
XM_011533687.2:c.6609C= XP_011531989.1:p.Val2203=
XM_011533688.2:c.6582C= XP_011531990.1:p.Val2194=
XM_011533690.2:c.6654C= XP_011531992.1:p.Val2218=
XM_017006357.2:c.6651C= XP_016861846.1:p.Val2217=
NM_001099952.3:c.6507C= NP_001093422.2:p.Val2169=
NM_002222.6:c.6462C= NP_002213.5:p.Val2154=
NM_001099952.4:c.6507C= NP_001093422.2:p.Val2169=
NM_001168272.2:c.6606C= NP_001161744.1:p.Val2202=
NM_001378452.1:c.6651C= MANE Select NP_001365381.1:p.Val2217=
NM_002222.7:c.6462C= NP_002213.5:p.Val2154=