Canonical Allele Identifier: CA351640463

Gene: ITPR1

Linked Data

• dbSNP Id: rs1277650530
• gnomAD v2: 3-4829650-C-T
• gnomAD v3: 3-4787966-C-T
• gnomAD v4: 3-4787966-C-T
• MyVariant Identifiers: chr3:g.4829650C>T (hg19) ; chr3:g.4787966C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.4787966C>T , CM000665.2:g.4787966C>T	GRCh38
NC_000003.11:g.4829650C>T , CM000665.1:g.4829650C>T	GRCh37
NC_000003.10:g.4804650C>T	NCBI36
NG_016144.1:g.299619C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000302640.13:c.6646C>T	ENSP00000306253.9:n.6646C>T
ENST00000354582.12:c.6611C>T	ENSP00000346595.8:p.Thr2204Ile
ENST00000443694.5:c.6590C>T	ENSP00000401671.2:p.Thr2197Ile
ENST00000354582.11:c.6611C>T	ENSP00000346595.8:p.Thr2204Ile
ENST00000357086.10:c.6491C>T	ENSP00000349597.4:p.Thr2164Ile
ENST00000443694.4:c.6590C>T	ENSP00000401671.2:p.Thr2197Ile
ENST00000456211.8:c.6446C>T	ENSP00000397885.2:p.Thr2149Ile
ENST00000481415.2:n.527C>T
ENST00000544951.6:c.997-18137C>T	ENSP00000440564.1:n.997-18137C>T
ENST00000647708.1:c.2534C>T
ENST00000647717.1:n.4139C>T
ENST00000648016.1:c.2970C>T
ENST00000648038.1:c.4397C>T	ENSP00000497872.1:p.Thr1466Ile
ENST00000648212.1:c.3543C>T
ENST00000648266.1:c.6608C>T	ENSP00000498014.1:p.Thr2203Ile
ENST00000648309.1:c.6563C>T	ENSP00000497026.1:p.Thr2188Ile
ENST00000648390.1:c.447-58173C>T
ENST00000648431.1:c.3937C>T
ENST00000648510.1:n.469C>T
ENST00000649015.2:c.6635C>T MANE Select	ENSP00000497605.1:p.Thr2212Ile
ENST00000649144.1:n.1683C>T
ENST00000649272.1:n.197C>T
ENST00000649694.1:n.4120C>T
ENST00000650294.1:c.6593C>T	ENSP00000498056.1:p.Thr2198Ile
ENST00000302640.12:c.6590C>T	ENSP00000306253.8:p.Thr2197Ile
ENST00000354582.10:c.6635C>T	ENSP00000346595.7:p.Thr2212Ile
ENST00000357086.9:c.6491C>T	ENSP00000349597.4:p.Thr2164Ile
ENST00000443694.3:c.6590C>T	ENSP00000401671.2:p.Thr2197Ile
ENST00000456211.7:c.6446C>T	ENSP00000397885.2:p.Thr2149Ile
ENST00000481415.1:n.527C>T
ENST00000544951.5:c.997-18137C>T	ENSP00000440564.1:n.997-18137C>T
NM_001099952.2:c.6491C>T	NP_001093422.2:p.Thr2164Ile
NM_001168272.1:c.6590C>T	NP_001161744.1:p.Thr2197Ile
NM_002222.5:c.6446C>T	NP_002213.5:p.Thr2149Ile
XM_005265109.2:c.6566C>T	XP_005265166.1:p.Thr2189Ile
XM_005265110.2:c.6518C>T	XP_005265167.1:p.Thr2173Ile
XM_006713131.2:c.6569C>T	XP_006713194.1:p.Thr2190Ile
XM_011533681.1:c.6638C>T	XP_011531983.1:p.Thr2213Ile
XM_011533682.1:c.6638C>T	XP_011531984.1:p.Thr2213Ile
XM_011533683.1:c.6635C>T	XP_011531985.1:p.Thr2212Ile
XM_011533684.1:c.6611C>T	XP_011531986.1:p.Thr2204Ile
XM_011533685.1:c.6605C>T	XP_011531987.1:p.Thr2202Ile
XM_011533686.1:c.6602C>T	XP_011531988.1:p.Thr2201Ile
XM_011533687.1:c.6593C>T	XP_011531989.1:p.Thr2198Ile
XM_011533688.1:c.6566C>T	XP_011531990.1:p.Thr2189Ile
XM_011533689.1:c.6527C>T	XP_011531991.1:p.Thr2176Ile
XM_011533690.1:c.6638C>T	XP_011531992.1:p.Thr2213Ile
XM_005265109.3:c.6566C>T	XP_005265166.1:p.Thr2189Ile
XM_005265110.3:c.6518C>T	XP_005265167.1:p.Thr2173Ile
XM_006713131.3:c.6569C>T	XP_006713194.1:p.Thr2190Ile
XM_011533682.3:c.6638C>T	XP_011531984.1:p.Thr2213Ile
XM_011533683.3:c.6635C>T	XP_011531985.1:p.Thr2212Ile
XM_011533684.2:c.6611C>T	XP_011531986.1:p.Thr2204Ile
XM_011533685.2:c.6605C>T	XP_011531987.1:p.Thr2202Ile
XM_011533686.2:c.6602C>T	XP_011531988.1:p.Thr2201Ile
XM_011533687.2:c.6593C>T	XP_011531989.1:p.Thr2198Ile
XM_011533688.2:c.6566C>T	XP_011531990.1:p.Thr2189Ile
XM_011533690.2:c.6638C>T	XP_011531992.1:p.Thr2213Ile
XM_017006357.2:c.6635C>T	XP_016861846.1:p.Thr2212Ile
NM_001099952.3:c.6491C>T	NP_001093422.2:p.Thr2164Ile
NM_002222.6:c.6446C>T	NP_002213.5:p.Thr2149Ile
NM_001099952.4:c.6491C>T	NP_001093422.2:p.Thr2164Ile
NM_001168272.2:c.6590C>T	NP_001161744.1:p.Thr2197Ile
NM_001378452.1:c.6635C>T MANE Select	NP_001365381.1:p.Thr2212Ile
NM_002222.7:c.6446C>T	NP_002213.5:p.Thr2149Ile