Canonical Allele Identifier: CA1342337451
Gene: ITPR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.4788077A= , CM000665.2:g.4788077A= GRCh38
NC_000003.11:g.4829761A= , CM000665.1:g.4829761A= GRCh37
NC_000003.10:g.4804761A= NCBI36
NG_016144.1:g.299730A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000302640.13:c.6757A= ENSP00000306253.9:n.6757A=
ENST00000354582.12:c.6722A= ENSP00000346595.8:p.Asn2241=
ENST00000443694.5:c.6701A= ENSP00000401671.2:p.Asn2234=
ENST00000354582.11:c.6722A= ENSP00000346595.8:p.Asn2241=
ENST00000357086.10:c.6602A= ENSP00000349597.4:p.Asn2201=
ENST00000443694.4:c.6701A= ENSP00000401671.2:p.Asn2234=
ENST00000456211.8:c.6557A= ENSP00000397885.2:p.Asn2186=
ENST00000481415.2:n.638A=
ENST00000544951.6:c.997-18026A= ENSP00000440564.1:n.997-18026A=
ENST00000647708.1:c.2645A=
ENST00000647717.1:n.4250A=
ENST00000648016.1:c.3081A=
ENST00000648038.1:c.4508A= ENSP00000497872.1:p.Asn1503=
ENST00000648212.1:c.3654A=
ENST00000648266.1:c.6719A= ENSP00000498014.1:p.Asn2240=
ENST00000648309.1:c.6674A= ENSP00000497026.1:p.Asn2225=
ENST00000648390.1:c.447-58062A=
ENST00000648431.1:c.4048A=
ENST00000648510.1:n.580A=
ENST00000649015.2:c.6746A= MANE Select ENSP00000497605.1:p.Asn2249=
ENST00000649144.1:n.1794A=
ENST00000649272.1:n.308A=
ENST00000649694.1:n.4231A=
ENST00000650294.1:c.6704A= ENSP00000498056.1:p.Asn2235=
ENST00000302640.12:c.6701A= ENSP00000306253.8:p.Asn2234=
ENST00000354582.10:c.6746A= ENSP00000346595.7:p.Asn2249=
ENST00000357086.9:c.6602A= ENSP00000349597.4:p.Asn2201=
ENST00000443694.3:c.6701A= ENSP00000401671.2:p.Asn2234=
ENST00000456211.7:c.6557A= ENSP00000397885.2:p.Asn2186=
ENST00000544951.5:c.997-18026A= ENSP00000440564.1:n.997-18026A=
NM_001099952.2:c.6602A= NP_001093422.2:p.Asn2201=
NM_001168272.1:c.6701A= NP_001161744.1:p.Asn2234=
NM_002222.5:c.6557A= NP_002213.5:p.Asn2186=
XM_005265109.2:c.6677A= XP_005265166.1:p.Asn2226=
XM_005265110.2:c.6629A= XP_005265167.1:p.Asn2210=
XM_006713131.2:c.6680A= XP_006713194.1:p.Asn2227=
XM_011533681.1:c.6749A= XP_011531983.1:p.Asn2250=
XM_011533682.1:c.6749A= XP_011531984.1:p.Asn2250=
XM_011533683.1:c.6746A= XP_011531985.1:p.Asn2249=
XM_011533684.1:c.6722A= XP_011531986.1:p.Asn2241=
XM_011533685.1:c.6716A= XP_011531987.1:p.Asn2239=
XM_011533686.1:c.6713A= XP_011531988.1:p.Asn2238=
XM_011533687.1:c.6704A= XP_011531989.1:p.Asn2235=
XM_011533688.1:c.6677A= XP_011531990.1:p.Asn2226=
XM_011533689.1:c.6638A= XP_011531991.1:p.Asn2213=
XM_011533690.1:c.6749A= XP_011531992.1:p.Asn2250=
XM_005265109.3:c.6677A= XP_005265166.1:p.Asn2226=
XM_005265110.3:c.6629A= XP_005265167.1:p.Asn2210=
XM_006713131.3:c.6680A= XP_006713194.1:p.Asn2227=
XM_011533682.3:c.6749A= XP_011531984.1:p.Asn2250=
XM_011533683.3:c.6746A= XP_011531985.1:p.Asn2249=
XM_011533684.2:c.6722A= XP_011531986.1:p.Asn2241=
XM_011533685.2:c.6716A= XP_011531987.1:p.Asn2239=
XM_011533686.2:c.6713A= XP_011531988.1:p.Asn2238=
XM_011533687.2:c.6704A= XP_011531989.1:p.Asn2235=
XM_011533688.2:c.6677A= XP_011531990.1:p.Asn2226=
XM_011533690.2:c.6749A= XP_011531992.1:p.Asn2250=
XM_017006357.2:c.6746A= XP_016861846.1:p.Asn2249=
NM_001099952.3:c.6602A= NP_001093422.2:p.Asn2201=
NM_002222.6:c.6557A= NP_002213.5:p.Asn2186=
NM_001099952.4:c.6602A= NP_001093422.2:p.Asn2201=
NM_001168272.2:c.6701A= NP_001161744.1:p.Asn2234=
NM_001378452.1:c.6746A= MANE Select NP_001365381.1:p.Asn2249=
NM_002222.7:c.6557A= NP_002213.5:p.Asn2186=