Canonical Allele Identifier: CA351640802

Gene: ITPR1

Linked Data

• gnomAD v4: 3-4788101-A-C
• MyVariant Identifiers: chr3:g.4829785A>C (hg19) ; chr3:g.4788101A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.4788101A>C , CM000665.2:g.4788101A>C	GRCh38
NC_000003.11:g.4829785A>C , CM000665.1:g.4829785A>C	GRCh37
NC_000003.10:g.4804785A>C	NCBI36
NG_016144.1:g.299754A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302640.13:c.6781A>C	ENSP00000306253.9:n.6781A>C
ENST00000354582.12:c.6746A>C	ENSP00000346595.8:p.Asp2249Ala
ENST00000443694.5:c.6725A>C	ENSP00000401671.2:p.Asp2242Ala
ENST00000354582.11:c.6746A>C	ENSP00000346595.8:p.Asp2249Ala
ENST00000357086.10:c.6626A>C	ENSP00000349597.4:p.Asp2209Ala
ENST00000443694.4:c.6725A>C	ENSP00000401671.2:p.Asp2242Ala
ENST00000456211.8:c.6581A>C	ENSP00000397885.2:p.Asp2194Ala
ENST00000481415.2:n.662A>C
ENST00000544951.6:c.997-18002A>C	ENSP00000440564.1:n.997-18002A>C
ENST00000647708.1:c.2669A>C
ENST00000647717.1:n.4274A>C
ENST00000648016.1:c.3105A>C
ENST00000648038.1:c.4532A>C	ENSP00000497872.1:p.Asp1511Ala
ENST00000648212.1:c.3678A>C
ENST00000648266.1:c.6743A>C	ENSP00000498014.1:p.Asp2248Ala
ENST00000648309.1:c.6698A>C	ENSP00000497026.1:p.Asp2233Ala
ENST00000648390.1:c.447-58038A>C
ENST00000648431.1:c.4072A>C
ENST00000648510.1:n.604A>C
ENST00000649015.2:c.6770A>C MANE Select	ENSP00000497605.1:p.Asp2257Ala
ENST00000649144.1:n.1818A>C
ENST00000649272.1:n.332A>C
ENST00000649694.1:n.4255A>C
ENST00000650294.1:c.6728A>C	ENSP00000498056.1:p.Asp2243Ala
ENST00000302640.12:c.6725A>C	ENSP00000306253.8:p.Asp2242Ala
ENST00000354582.10:c.6770A>C	ENSP00000346595.7:p.Asp2257Ala
ENST00000357086.9:c.6626A>C	ENSP00000349597.4:p.Asp2209Ala
ENST00000443694.3:c.6725A>C	ENSP00000401671.2:p.Asp2242Ala
ENST00000456211.7:c.6581A>C	ENSP00000397885.2:p.Asp2194Ala
ENST00000544951.5:c.997-18002A>C	ENSP00000440564.1:n.997-18002A>C
NM_001099952.2:c.6626A>C	NP_001093422.2:p.Asp2209Ala
NM_001168272.1:c.6725A>C	NP_001161744.1:p.Asp2242Ala
NM_002222.5:c.6581A>C	NP_002213.5:p.Asp2194Ala
XM_005265109.2:c.6701A>C	XP_005265166.1:p.Asp2234Ala
XM_005265110.2:c.6653A>C	XP_005265167.1:p.Asp2218Ala
XM_006713131.2:c.6704A>C	XP_006713194.1:p.Asp2235Ala
XM_011533681.1:c.6773A>C	XP_011531983.1:p.Asp2258Ala
XM_011533682.1:c.6773A>C	XP_011531984.1:p.Asp2258Ala
XM_011533683.1:c.6770A>C	XP_011531985.1:p.Asp2257Ala
XM_011533684.1:c.6746A>C	XP_011531986.1:p.Asp2249Ala
XM_011533685.1:c.6740A>C	XP_011531987.1:p.Asp2247Ala
XM_011533686.1:c.6737A>C	XP_011531988.1:p.Asp2246Ala
XM_011533687.1:c.6728A>C	XP_011531989.1:p.Asp2243Ala
XM_011533688.1:c.6701A>C	XP_011531990.1:p.Asp2234Ala
XM_011533689.1:c.6662A>C	XP_011531991.1:p.Asp2221Ala
XM_011533690.1:c.6773A>C	XP_011531992.1:p.Asp2258Ala
XM_005265109.3:c.6701A>C	XP_005265166.1:p.Asp2234Ala
XM_005265110.3:c.6653A>C	XP_005265167.1:p.Asp2218Ala
XM_006713131.3:c.6704A>C	XP_006713194.1:p.Asp2235Ala
XM_011533682.3:c.6773A>C	XP_011531984.1:p.Asp2258Ala
XM_011533683.3:c.6770A>C	XP_011531985.1:p.Asp2257Ala
XM_011533684.2:c.6746A>C	XP_011531986.1:p.Asp2249Ala
XM_011533685.2:c.6740A>C	XP_011531987.1:p.Asp2247Ala
XM_011533686.2:c.6737A>C	XP_011531988.1:p.Asp2246Ala
XM_011533687.2:c.6728A>C	XP_011531989.1:p.Asp2243Ala
XM_011533688.2:c.6701A>C	XP_011531990.1:p.Asp2234Ala
XM_011533690.2:c.6773A>C	XP_011531992.1:p.Asp2258Ala
XM_017006357.2:c.6770A>C	XP_016861846.1:p.Asp2257Ala
NM_001099952.3:c.6626A>C	NP_001093422.2:p.Asp2209Ala
NM_002222.6:c.6581A>C	NP_002213.5:p.Asp2194Ala
NM_001099952.4:c.6626A>C	NP_001093422.2:p.Asp2209Ala
NM_001168272.2:c.6725A>C	NP_001161744.1:p.Asp2242Ala
NM_001378452.1:c.6770A>C MANE Select	NP_001365381.1:p.Asp2257Ala
NM_002222.7:c.6581A>C	NP_002213.5:p.Asp2194Ala