Canonical Allele Identifier: CA351640559

Gene: ITPR1

Linked Data

• MyVariant Identifiers: chr3:g.4829692T>A (hg19) ; chr3:g.4788008T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.4788008T>A , CM000665.2:g.4788008T>A	GRCh38
NC_000003.11:g.4829692T>A , CM000665.1:g.4829692T>A	GRCh37
NC_000003.10:g.4804692T>A	NCBI36
NG_016144.1:g.299661T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302640.13:c.6688T>A	ENSP00000306253.9:n.6688T>A
ENST00000354582.12:c.6653T>A	ENSP00000346595.8:p.Phe2218Tyr
ENST00000443694.5:c.6632T>A	ENSP00000401671.2:p.Phe2211Tyr
ENST00000354582.11:c.6653T>A	ENSP00000346595.8:p.Phe2218Tyr
ENST00000357086.10:c.6533T>A	ENSP00000349597.4:p.Phe2178Tyr
ENST00000443694.4:c.6632T>A	ENSP00000401671.2:p.Phe2211Tyr
ENST00000456211.8:c.6488T>A	ENSP00000397885.2:p.Phe2163Tyr
ENST00000481415.2:n.569T>A
ENST00000544951.6:c.997-18095T>A	ENSP00000440564.1:n.997-18095T>A
ENST00000647708.1:c.2576T>A
ENST00000647717.1:n.4181T>A
ENST00000648016.1:c.3012T>A
ENST00000648038.1:c.4439T>A	ENSP00000497872.1:p.Phe1480Tyr
ENST00000648212.1:c.3585T>A
ENST00000648266.1:c.6650T>A	ENSP00000498014.1:p.Phe2217Tyr
ENST00000648309.1:c.6605T>A	ENSP00000497026.1:p.Phe2202Tyr
ENST00000648390.1:c.447-58131T>A
ENST00000648431.1:c.3979T>A
ENST00000648510.1:n.511T>A
ENST00000649015.2:c.6677T>A MANE Select	ENSP00000497605.1:p.Phe2226Tyr
ENST00000649144.1:n.1725T>A
ENST00000649272.1:n.239T>A
ENST00000649694.1:n.4162T>A
ENST00000650294.1:c.6635T>A	ENSP00000498056.1:p.Phe2212Tyr
ENST00000302640.12:c.6632T>A	ENSP00000306253.8:p.Phe2211Tyr
ENST00000354582.10:c.6677T>A	ENSP00000346595.7:p.Phe2226Tyr
ENST00000357086.9:c.6533T>A	ENSP00000349597.4:p.Phe2178Tyr
ENST00000443694.3:c.6632T>A	ENSP00000401671.2:p.Phe2211Tyr
ENST00000456211.7:c.6488T>A	ENSP00000397885.2:p.Phe2163Tyr
ENST00000544951.5:c.997-18095T>A	ENSP00000440564.1:n.997-18095T>A
NM_001099952.2:c.6533T>A	NP_001093422.2:p.Phe2178Tyr
NM_001168272.1:c.6632T>A	NP_001161744.1:p.Phe2211Tyr
NM_002222.5:c.6488T>A	NP_002213.5:p.Phe2163Tyr
XM_005265109.2:c.6608T>A	XP_005265166.1:p.Phe2203Tyr
XM_005265110.2:c.6560T>A	XP_005265167.1:p.Phe2187Tyr
XM_006713131.2:c.6611T>A	XP_006713194.1:p.Phe2204Tyr
XM_011533681.1:c.6680T>A	XP_011531983.1:p.Phe2227Tyr
XM_011533682.1:c.6680T>A	XP_011531984.1:p.Phe2227Tyr
XM_011533683.1:c.6677T>A	XP_011531985.1:p.Phe2226Tyr
XM_011533684.1:c.6653T>A	XP_011531986.1:p.Phe2218Tyr
XM_011533685.1:c.6647T>A	XP_011531987.1:p.Phe2216Tyr
XM_011533686.1:c.6644T>A	XP_011531988.1:p.Phe2215Tyr
XM_011533687.1:c.6635T>A	XP_011531989.1:p.Phe2212Tyr
XM_011533688.1:c.6608T>A	XP_011531990.1:p.Phe2203Tyr
XM_011533689.1:c.6569T>A	XP_011531991.1:p.Phe2190Tyr
XM_011533690.1:c.6680T>A	XP_011531992.1:p.Phe2227Tyr
XM_005265109.3:c.6608T>A	XP_005265166.1:p.Phe2203Tyr
XM_005265110.3:c.6560T>A	XP_005265167.1:p.Phe2187Tyr
XM_006713131.3:c.6611T>A	XP_006713194.1:p.Phe2204Tyr
XM_011533682.3:c.6680T>A	XP_011531984.1:p.Phe2227Tyr
XM_011533683.3:c.6677T>A	XP_011531985.1:p.Phe2226Tyr
XM_011533684.2:c.6653T>A	XP_011531986.1:p.Phe2218Tyr
XM_011533685.2:c.6647T>A	XP_011531987.1:p.Phe2216Tyr
XM_011533686.2:c.6644T>A	XP_011531988.1:p.Phe2215Tyr
XM_011533687.2:c.6635T>A	XP_011531989.1:p.Phe2212Tyr
XM_011533688.2:c.6608T>A	XP_011531990.1:p.Phe2203Tyr
XM_011533690.2:c.6680T>A	XP_011531992.1:p.Phe2227Tyr
XM_017006357.2:c.6677T>A	XP_016861846.1:p.Phe2226Tyr
NM_001099952.3:c.6533T>A	NP_001093422.2:p.Phe2178Tyr
NM_002222.6:c.6488T>A	NP_002213.5:p.Phe2163Tyr
NM_001099952.4:c.6533T>A	NP_001093422.2:p.Phe2178Tyr
NM_001168272.2:c.6632T>A	NP_001161744.1:p.Phe2211Tyr
NM_001378452.1:c.6677T>A MANE Select	NP_001365381.1:p.Phe2226Tyr
NM_002222.7:c.6488T>A	NP_002213.5:p.Phe2163Tyr