Canonical Allele Identifier: CA351640627

Gene: ITPR1

Linked Data

• MyVariant Identifiers: chr3:g.4829723C>G (hg19) ; chr3:g.4788039C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.4788039C>G , CM000665.2:g.4788039C>G	GRCh38
NC_000003.11:g.4829723C>G , CM000665.1:g.4829723C>G	GRCh37
NC_000003.10:g.4804723C>G	NCBI36
NG_016144.1:g.299692C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302640.13:c.6719C>G	ENSP00000306253.9:n.6719C>G
ENST00000354582.12:c.6684C>G	ENSP00000346595.8:p.Tyr2228Ter
ENST00000443694.5:c.6663C>G	ENSP00000401671.2:p.Tyr2221Ter
ENST00000354582.11:c.6684C>G	ENSP00000346595.8:p.Tyr2228Ter
ENST00000357086.10:c.6564C>G	ENSP00000349597.4:p.Tyr2188Ter
ENST00000443694.4:c.6663C>G	ENSP00000401671.2:p.Tyr2221Ter
ENST00000456211.8:c.6519C>G	ENSP00000397885.2:p.Tyr2173Ter
ENST00000481415.2:n.600C>G
ENST00000544951.6:c.997-18064C>G	ENSP00000440564.1:n.997-18064C>G
ENST00000647708.1:c.2607C>G
ENST00000647717.1:n.4212C>G
ENST00000648016.1:c.3043C>G
ENST00000648038.1:c.4470C>G	ENSP00000497872.1:p.Tyr1490Ter
ENST00000648212.1:c.3616C>G
ENST00000648266.1:c.6681C>G	ENSP00000498014.1:p.Tyr2227Ter
ENST00000648309.1:c.6636C>G	ENSP00000497026.1:p.Tyr2212Ter
ENST00000648390.1:c.447-58100C>G
ENST00000648431.1:c.4010C>G
ENST00000648510.1:n.542C>G
ENST00000649015.2:c.6708C>G MANE Select	ENSP00000497605.1:p.Tyr2236Ter
ENST00000649144.1:n.1756C>G
ENST00000649272.1:n.270C>G
ENST00000649694.1:n.4193C>G
ENST00000650294.1:c.6666C>G	ENSP00000498056.1:p.Tyr2222Ter
ENST00000302640.12:c.6663C>G	ENSP00000306253.8:p.Tyr2221Ter
ENST00000354582.10:c.6708C>G	ENSP00000346595.7:p.Tyr2236Ter
ENST00000357086.9:c.6564C>G	ENSP00000349597.4:p.Tyr2188Ter
ENST00000443694.3:c.6663C>G	ENSP00000401671.2:p.Tyr2221Ter
ENST00000456211.7:c.6519C>G	ENSP00000397885.2:p.Tyr2173Ter
ENST00000544951.5:c.997-18064C>G	ENSP00000440564.1:n.997-18064C>G
NM_001099952.2:c.6564C>G	NP_001093422.2:p.Tyr2188Ter
NM_001168272.1:c.6663C>G	NP_001161744.1:p.Tyr2221Ter
NM_002222.5:c.6519C>G	NP_002213.5:p.Tyr2173Ter
XM_005265109.2:c.6639C>G	XP_005265166.1:p.Tyr2213Ter
XM_005265110.2:c.6591C>G	XP_005265167.1:p.Tyr2197Ter
XM_006713131.2:c.6642C>G	XP_006713194.1:p.Tyr2214Ter
XM_011533681.1:c.6711C>G	XP_011531983.1:p.Tyr2237Ter
XM_011533682.1:c.6711C>G	XP_011531984.1:p.Tyr2237Ter
XM_011533683.1:c.6708C>G	XP_011531985.1:p.Tyr2236Ter
XM_011533684.1:c.6684C>G	XP_011531986.1:p.Tyr2228Ter
XM_011533685.1:c.6678C>G	XP_011531987.1:p.Tyr2226Ter
XM_011533686.1:c.6675C>G	XP_011531988.1:p.Tyr2225Ter
XM_011533687.1:c.6666C>G	XP_011531989.1:p.Tyr2222Ter
XM_011533688.1:c.6639C>G	XP_011531990.1:p.Tyr2213Ter
XM_011533689.1:c.6600C>G	XP_011531991.1:p.Tyr2200Ter
XM_011533690.1:c.6711C>G	XP_011531992.1:p.Tyr2237Ter
XM_005265109.3:c.6639C>G	XP_005265166.1:p.Tyr2213Ter
XM_005265110.3:c.6591C>G	XP_005265167.1:p.Tyr2197Ter
XM_006713131.3:c.6642C>G	XP_006713194.1:p.Tyr2214Ter
XM_011533682.3:c.6711C>G	XP_011531984.1:p.Tyr2237Ter
XM_011533683.3:c.6708C>G	XP_011531985.1:p.Tyr2236Ter
XM_011533684.2:c.6684C>G	XP_011531986.1:p.Tyr2228Ter
XM_011533685.2:c.6678C>G	XP_011531987.1:p.Tyr2226Ter
XM_011533686.2:c.6675C>G	XP_011531988.1:p.Tyr2225Ter
XM_011533687.2:c.6666C>G	XP_011531989.1:p.Tyr2222Ter
XM_011533688.2:c.6639C>G	XP_011531990.1:p.Tyr2213Ter
XM_011533690.2:c.6711C>G	XP_011531992.1:p.Tyr2237Ter
XM_017006357.2:c.6708C>G	XP_016861846.1:p.Tyr2236Ter
NM_001099952.3:c.6564C>G	NP_001093422.2:p.Tyr2188Ter
NM_002222.6:c.6519C>G	NP_002213.5:p.Tyr2173Ter
NM_001099952.4:c.6564C>G	NP_001093422.2:p.Tyr2188Ter
NM_001168272.2:c.6663C>G	NP_001161744.1:p.Tyr2221Ter
NM_001378452.1:c.6708C>G MANE Select	NP_001365381.1:p.Tyr2236Ter
NM_002222.7:c.6519C>G	NP_002213.5:p.Tyr2173Ter