Canonical Allele Identifier: CA1342337412
Gene: ITPR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.4787962C= , CM000665.2:g.4787962C= GRCh38
NC_000003.11:g.4829646C= , CM000665.1:g.4829646C= GRCh37
NC_000003.10:g.4804646C= NCBI36
NG_016144.1:g.299615C=

Transcript Alleles

HGVS Amino-acid change
ENST00000302640.13:c.6642C= ENSP00000306253.9:n.6642C=
ENST00000354582.12:c.6607C= ENSP00000346595.8:p.Arg2203=
ENST00000443694.5:c.6586C= ENSP00000401671.2:p.Arg2196=
ENST00000354582.11:c.6607C= ENSP00000346595.8:p.Arg2203=
ENST00000357086.10:c.6487C= ENSP00000349597.4:p.Arg2163=
ENST00000443694.4:c.6586C= ENSP00000401671.2:p.Arg2196=
ENST00000456211.8:c.6442C= ENSP00000397885.2:p.Arg2148=
ENST00000481415.2:n.523C=
ENST00000544951.6:c.997-18141C= ENSP00000440564.1:n.997-18141C=
ENST00000647708.1:c.2530C=
ENST00000647717.1:n.4135C=
ENST00000648016.1:c.2966C=
ENST00000648038.1:c.4393C= ENSP00000497872.1:p.Arg1465=
ENST00000648212.1:c.3539C=
ENST00000648266.1:c.6604C= ENSP00000498014.1:p.Arg2202=
ENST00000648309.1:c.6559C= ENSP00000497026.1:p.Arg2187=
ENST00000648390.1:c.447-58177C=
ENST00000648431.1:c.3933C=
ENST00000648510.1:n.465C=
ENST00000649015.2:c.6631C= MANE Select ENSP00000497605.1:p.Arg2211=
ENST00000649144.1:n.1679C=
ENST00000649272.1:n.193C=
ENST00000649694.1:n.4116C=
ENST00000650294.1:c.6589C= ENSP00000498056.1:p.Arg2197=
ENST00000302640.12:c.6586C= ENSP00000306253.8:p.Arg2196=
ENST00000354582.10:c.6631C= ENSP00000346595.7:p.Arg2211=
ENST00000357086.9:c.6487C= ENSP00000349597.4:p.Arg2163=
ENST00000443694.3:c.6586C= ENSP00000401671.2:p.Arg2196=
ENST00000456211.7:c.6442C= ENSP00000397885.2:p.Arg2148=
ENST00000481415.1:n.523C=
ENST00000544951.5:c.997-18141C= ENSP00000440564.1:n.997-18141C=
NM_001099952.2:c.6487C= NP_001093422.2:p.Arg2163=
NM_001168272.1:c.6586C= NP_001161744.1:p.Arg2196=
NM_002222.5:c.6442C= NP_002213.5:p.Arg2148=
XM_005265109.2:c.6562C= XP_005265166.1:p.Arg2188=
XM_005265110.2:c.6514C= XP_005265167.1:p.Arg2172=
XM_006713131.2:c.6565C= XP_006713194.1:p.Arg2189=
XM_011533681.1:c.6634C= XP_011531983.1:p.Arg2212=
XM_011533682.1:c.6634C= XP_011531984.1:p.Arg2212=
XM_011533683.1:c.6631C= XP_011531985.1:p.Arg2211=
XM_011533684.1:c.6607C= XP_011531986.1:p.Arg2203=
XM_011533685.1:c.6601C= XP_011531987.1:p.Arg2201=
XM_011533686.1:c.6598C= XP_011531988.1:p.Arg2200=
XM_011533687.1:c.6589C= XP_011531989.1:p.Arg2197=
XM_011533688.1:c.6562C= XP_011531990.1:p.Arg2188=
XM_011533689.1:c.6523C= XP_011531991.1:p.Arg2175=
XM_011533690.1:c.6634C= XP_011531992.1:p.Arg2212=
XM_005265109.3:c.6562C= XP_005265166.1:p.Arg2188=
XM_005265110.3:c.6514C= XP_005265167.1:p.Arg2172=
XM_006713131.3:c.6565C= XP_006713194.1:p.Arg2189=
XM_011533682.3:c.6634C= XP_011531984.1:p.Arg2212=
XM_011533683.3:c.6631C= XP_011531985.1:p.Arg2211=
XM_011533684.2:c.6607C= XP_011531986.1:p.Arg2203=
XM_011533685.2:c.6601C= XP_011531987.1:p.Arg2201=
XM_011533686.2:c.6598C= XP_011531988.1:p.Arg2200=
XM_011533687.2:c.6589C= XP_011531989.1:p.Arg2197=
XM_011533688.2:c.6562C= XP_011531990.1:p.Arg2188=
XM_011533690.2:c.6634C= XP_011531992.1:p.Arg2212=
XM_017006357.2:c.6631C= XP_016861846.1:p.Arg2211=
NM_001099952.3:c.6487C= NP_001093422.2:p.Arg2163=
NM_002222.6:c.6442C= NP_002213.5:p.Arg2148=
NM_001099952.4:c.6487C= NP_001093422.2:p.Arg2163=
NM_001168272.2:c.6586C= NP_001161744.1:p.Arg2196=
NM_001378452.1:c.6631C= MANE Select NP_001365381.1:p.Arg2211=
NM_002222.7:c.6442C= NP_002213.5:p.Arg2148=