Canonical Allele Identifier: CA1342337433
Gene: ITPR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.4788028C= , CM000665.2:g.4788028C= GRCh38
NC_000003.11:g.4829712C= , CM000665.1:g.4829712C= GRCh37
NC_000003.10:g.4804712C= NCBI36
NG_016144.1:g.299681C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000302640.13:c.6708C= ENSP00000306253.9:n.6708C=
ENST00000354582.12:c.6673C= ENSP00000346595.8:p.Leu2225=
ENST00000443694.5:c.6652C= ENSP00000401671.2:p.Leu2218=
ENST00000354582.11:c.6673C= ENSP00000346595.8:p.Leu2225=
ENST00000357086.10:c.6553C= ENSP00000349597.4:p.Leu2185=
ENST00000443694.4:c.6652C= ENSP00000401671.2:p.Leu2218=
ENST00000456211.8:c.6508C= ENSP00000397885.2:p.Leu2170=
ENST00000481415.2:n.589C=
ENST00000544951.6:c.997-18075C= ENSP00000440564.1:n.997-18075C=
ENST00000647708.1:c.2596C=
ENST00000647717.1:n.4201C=
ENST00000648016.1:c.3032C=
ENST00000648038.1:c.4459C= ENSP00000497872.1:p.Leu1487=
ENST00000648212.1:c.3605C=
ENST00000648266.1:c.6670C= ENSP00000498014.1:p.Leu2224=
ENST00000648309.1:c.6625C= ENSP00000497026.1:p.Leu2209=
ENST00000648390.1:c.447-58111C=
ENST00000648431.1:c.3999C=
ENST00000648510.1:n.531C=
ENST00000649015.2:c.6697C= MANE Select ENSP00000497605.1:p.Leu2233=
ENST00000649144.1:n.1745C=
ENST00000649272.1:n.259C=
ENST00000649694.1:n.4182C=
ENST00000650294.1:c.6655C= ENSP00000498056.1:p.Leu2219=
ENST00000302640.12:c.6652C= ENSP00000306253.8:p.Leu2218=
ENST00000354582.10:c.6697C= ENSP00000346595.7:p.Leu2233=
ENST00000357086.9:c.6553C= ENSP00000349597.4:p.Leu2185=
ENST00000443694.3:c.6652C= ENSP00000401671.2:p.Leu2218=
ENST00000456211.7:c.6508C= ENSP00000397885.2:p.Leu2170=
ENST00000544951.5:c.997-18075C= ENSP00000440564.1:n.997-18075C=
NM_001099952.2:c.6553C= NP_001093422.2:p.Leu2185=
NM_001168272.1:c.6652C= NP_001161744.1:p.Leu2218=
NM_002222.5:c.6508C= NP_002213.5:p.Leu2170=
XM_005265109.2:c.6628C= XP_005265166.1:p.Leu2210=
XM_005265110.2:c.6580C= XP_005265167.1:p.Leu2194=
XM_006713131.2:c.6631C= XP_006713194.1:p.Leu2211=
XM_011533681.1:c.6700C= XP_011531983.1:p.Leu2234=
XM_011533682.1:c.6700C= XP_011531984.1:p.Leu2234=
XM_011533683.1:c.6697C= XP_011531985.1:p.Leu2233=
XM_011533684.1:c.6673C= XP_011531986.1:p.Leu2225=
XM_011533685.1:c.6667C= XP_011531987.1:p.Leu2223=
XM_011533686.1:c.6664C= XP_011531988.1:p.Leu2222=
XM_011533687.1:c.6655C= XP_011531989.1:p.Leu2219=
XM_011533688.1:c.6628C= XP_011531990.1:p.Leu2210=
XM_011533689.1:c.6589C= XP_011531991.1:p.Leu2197=
XM_011533690.1:c.6700C= XP_011531992.1:p.Leu2234=
XM_005265109.3:c.6628C= XP_005265166.1:p.Leu2210=
XM_005265110.3:c.6580C= XP_005265167.1:p.Leu2194=
XM_006713131.3:c.6631C= XP_006713194.1:p.Leu2211=
XM_011533682.3:c.6700C= XP_011531984.1:p.Leu2234=
XM_011533683.3:c.6697C= XP_011531985.1:p.Leu2233=
XM_011533684.2:c.6673C= XP_011531986.1:p.Leu2225=
XM_011533685.2:c.6667C= XP_011531987.1:p.Leu2223=
XM_011533686.2:c.6664C= XP_011531988.1:p.Leu2222=
XM_011533687.2:c.6655C= XP_011531989.1:p.Leu2219=
XM_011533688.2:c.6628C= XP_011531990.1:p.Leu2210=
XM_011533690.2:c.6700C= XP_011531992.1:p.Leu2234=
XM_017006357.2:c.6697C= XP_016861846.1:p.Leu2233=
NM_001099952.3:c.6553C= NP_001093422.2:p.Leu2185=
NM_002222.6:c.6508C= NP_002213.5:p.Leu2170=
NM_001099952.4:c.6553C= NP_001093422.2:p.Leu2185=
NM_001168272.2:c.6652C= NP_001161744.1:p.Leu2218=
NM_001378452.1:c.6697C= MANE Select NP_001365381.1:p.Leu2233=
NM_002222.7:c.6508C= NP_002213.5:p.Leu2170=