Canonical Allele Identifier: CA351640621

Gene: ITPR1

Linked Data

• MyVariant Identifiers: chr3:g.4829721T>C (hg19) ; chr3:g.4788037T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.4788037T>C , CM000665.2:g.4788037T>C	GRCh38
NC_000003.11:g.4829721T>C , CM000665.1:g.4829721T>C	GRCh37
NC_000003.10:g.4804721T>C	NCBI36
NG_016144.1:g.299690T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302640.13:c.6717T>C	ENSP00000306253.9:n.6717T>C
ENST00000354582.12:c.6682T>C	ENSP00000346595.8:p.Tyr2228His
ENST00000443694.5:c.6661T>C	ENSP00000401671.2:p.Tyr2221His
ENST00000354582.11:c.6682T>C	ENSP00000346595.8:p.Tyr2228His
ENST00000357086.10:c.6562T>C	ENSP00000349597.4:p.Tyr2188His
ENST00000443694.4:c.6661T>C	ENSP00000401671.2:p.Tyr2221His
ENST00000456211.8:c.6517T>C	ENSP00000397885.2:p.Tyr2173His
ENST00000481415.2:n.598T>C
ENST00000544951.6:c.997-18066T>C	ENSP00000440564.1:n.997-18066T>C
ENST00000647708.1:c.2605T>C
ENST00000647717.1:n.4210T>C
ENST00000648016.1:c.3041T>C
ENST00000648038.1:c.4468T>C	ENSP00000497872.1:p.Tyr1490His
ENST00000648212.1:c.3614T>C
ENST00000648266.1:c.6679T>C	ENSP00000498014.1:p.Tyr2227His
ENST00000648309.1:c.6634T>C	ENSP00000497026.1:p.Tyr2212His
ENST00000648390.1:c.447-58102T>C
ENST00000648431.1:c.4008T>C
ENST00000648510.1:n.540T>C
ENST00000649015.2:c.6706T>C MANE Select	ENSP00000497605.1:p.Tyr2236His
ENST00000649144.1:n.1754T>C
ENST00000649272.1:n.268T>C
ENST00000649694.1:n.4191T>C
ENST00000650294.1:c.6664T>C	ENSP00000498056.1:p.Tyr2222His
ENST00000302640.12:c.6661T>C	ENSP00000306253.8:p.Tyr2221His
ENST00000354582.10:c.6706T>C	ENSP00000346595.7:p.Tyr2236His
ENST00000357086.9:c.6562T>C	ENSP00000349597.4:p.Tyr2188His
ENST00000443694.3:c.6661T>C	ENSP00000401671.2:p.Tyr2221His
ENST00000456211.7:c.6517T>C	ENSP00000397885.2:p.Tyr2173His
ENST00000544951.5:c.997-18066T>C	ENSP00000440564.1:n.997-18066T>C
NM_001099952.2:c.6562T>C	NP_001093422.2:p.Tyr2188His
NM_001168272.1:c.6661T>C	NP_001161744.1:p.Tyr2221His
NM_002222.5:c.6517T>C	NP_002213.5:p.Tyr2173His
XM_005265109.2:c.6637T>C	XP_005265166.1:p.Tyr2213His
XM_005265110.2:c.6589T>C	XP_005265167.1:p.Tyr2197His
XM_006713131.2:c.6640T>C	XP_006713194.1:p.Tyr2214His
XM_011533681.1:c.6709T>C	XP_011531983.1:p.Tyr2237His
XM_011533682.1:c.6709T>C	XP_011531984.1:p.Tyr2237His
XM_011533683.1:c.6706T>C	XP_011531985.1:p.Tyr2236His
XM_011533684.1:c.6682T>C	XP_011531986.1:p.Tyr2228His
XM_011533685.1:c.6676T>C	XP_011531987.1:p.Tyr2226His
XM_011533686.1:c.6673T>C	XP_011531988.1:p.Tyr2225His
XM_011533687.1:c.6664T>C	XP_011531989.1:p.Tyr2222His
XM_011533688.1:c.6637T>C	XP_011531990.1:p.Tyr2213His
XM_011533689.1:c.6598T>C	XP_011531991.1:p.Tyr2200His
XM_011533690.1:c.6709T>C	XP_011531992.1:p.Tyr2237His
XM_005265109.3:c.6637T>C	XP_005265166.1:p.Tyr2213His
XM_005265110.3:c.6589T>C	XP_005265167.1:p.Tyr2197His
XM_006713131.3:c.6640T>C	XP_006713194.1:p.Tyr2214His
XM_011533682.3:c.6709T>C	XP_011531984.1:p.Tyr2237His
XM_011533683.3:c.6706T>C	XP_011531985.1:p.Tyr2236His
XM_011533684.2:c.6682T>C	XP_011531986.1:p.Tyr2228His
XM_011533685.2:c.6676T>C	XP_011531987.1:p.Tyr2226His
XM_011533686.2:c.6673T>C	XP_011531988.1:p.Tyr2225His
XM_011533687.2:c.6664T>C	XP_011531989.1:p.Tyr2222His
XM_011533688.2:c.6637T>C	XP_011531990.1:p.Tyr2213His
XM_011533690.2:c.6709T>C	XP_011531992.1:p.Tyr2237His
XM_017006357.2:c.6706T>C	XP_016861846.1:p.Tyr2236His
NM_001099952.3:c.6562T>C	NP_001093422.2:p.Tyr2188His
NM_002222.6:c.6517T>C	NP_002213.5:p.Tyr2173His
NM_001099952.4:c.6562T>C	NP_001093422.2:p.Tyr2188His
NM_001168272.2:c.6661T>C	NP_001161744.1:p.Tyr2221His
NM_001378452.1:c.6706T>C MANE Select	NP_001365381.1:p.Tyr2236His
NM_002222.7:c.6517T>C	NP_002213.5:p.Tyr2173His