Canonical Allele Identifier: CA432322375

Gene: ITPR1

Linked Data

• gnomAD v4: 3-4787962-C-A
• MyVariant Identifiers: chr3:g.4829646C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.4787962C>A , CM000665.2:g.4787962C>A	GRCh38
NC_000003.11:g.4829646C>A , CM000665.1:g.4829646C>A	GRCh37
NC_000003.10:g.4804646C>A	NCBI36
NG_016144.1:g.299615C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000302640.13:c.6642C>A	ENSP00000306253.9:n.6642C>A
ENST00000354582.12:c.6607C>A	ENSP00000346595.8:p.Arg2203=
ENST00000443694.5:c.6586C>A	ENSP00000401671.2:p.Arg2196=
ENST00000354582.11:c.6607C>A	ENSP00000346595.8:p.Arg2203=
ENST00000357086.10:c.6487C>A	ENSP00000349597.4:p.Arg2163=
ENST00000443694.4:c.6586C>A	ENSP00000401671.2:p.Arg2196=
ENST00000456211.8:c.6442C>A	ENSP00000397885.2:p.Arg2148=
ENST00000481415.2:n.523C>A
ENST00000544951.6:c.997-18141C>A	ENSP00000440564.1:n.997-18141C>A
ENST00000647708.1:c.2530C>A
ENST00000647717.1:n.4135C>A
ENST00000648016.1:c.2966C>A
ENST00000648038.1:c.4393C>A	ENSP00000497872.1:p.Arg1465=
ENST00000648212.1:c.3539C>A
ENST00000648266.1:c.6604C>A	ENSP00000498014.1:p.Arg2202=
ENST00000648309.1:c.6559C>A	ENSP00000497026.1:p.Arg2187=
ENST00000648390.1:c.447-58177C>A
ENST00000648431.1:c.3933C>A
ENST00000648510.1:n.465C>A
ENST00000649015.2:c.6631C>A MANE Select	ENSP00000497605.1:p.Arg2211=
ENST00000649144.1:n.1679C>A
ENST00000649272.1:n.193C>A
ENST00000649694.1:n.4116C>A
ENST00000650294.1:c.6589C>A	ENSP00000498056.1:p.Arg2197=
ENST00000302640.12:c.6586C>A	ENSP00000306253.8:p.Arg2196=
ENST00000354582.10:c.6631C>A	ENSP00000346595.7:p.Arg2211=
ENST00000357086.9:c.6487C>A	ENSP00000349597.4:p.Arg2163=
ENST00000443694.3:c.6586C>A	ENSP00000401671.2:p.Arg2196=
ENST00000456211.7:c.6442C>A	ENSP00000397885.2:p.Arg2148=
ENST00000481415.1:n.523C>A
ENST00000544951.5:c.997-18141C>A	ENSP00000440564.1:n.997-18141C>A
NM_001099952.2:c.6487C>A	NP_001093422.2:p.Arg2163=
NM_001168272.1:c.6586C>A	NP_001161744.1:p.Arg2196=
NM_002222.5:c.6442C>A	NP_002213.5:p.Arg2148=
XM_005265109.2:c.6562C>A	XP_005265166.1:p.Arg2188=
XM_005265110.2:c.6514C>A	XP_005265167.1:p.Arg2172=
XM_006713131.2:c.6565C>A	XP_006713194.1:p.Arg2189=
XM_011533681.1:c.6634C>A	XP_011531983.1:p.Arg2212=
XM_011533682.1:c.6634C>A	XP_011531984.1:p.Arg2212=
XM_011533683.1:c.6631C>A	XP_011531985.1:p.Arg2211=
XM_011533684.1:c.6607C>A	XP_011531986.1:p.Arg2203=
XM_011533685.1:c.6601C>A	XP_011531987.1:p.Arg2201=
XM_011533686.1:c.6598C>A	XP_011531988.1:p.Arg2200=
XM_011533687.1:c.6589C>A	XP_011531989.1:p.Arg2197=
XM_011533688.1:c.6562C>A	XP_011531990.1:p.Arg2188=
XM_011533689.1:c.6523C>A	XP_011531991.1:p.Arg2175=
XM_011533690.1:c.6634C>A	XP_011531992.1:p.Arg2212=
XM_005265109.3:c.6562C>A	XP_005265166.1:p.Arg2188=
XM_005265110.3:c.6514C>A	XP_005265167.1:p.Arg2172=
XM_006713131.3:c.6565C>A	XP_006713194.1:p.Arg2189=
XM_011533682.3:c.6634C>A	XP_011531984.1:p.Arg2212=
XM_011533683.3:c.6631C>A	XP_011531985.1:p.Arg2211=
XM_011533684.2:c.6607C>A	XP_011531986.1:p.Arg2203=
XM_011533685.2:c.6601C>A	XP_011531987.1:p.Arg2201=
XM_011533686.2:c.6598C>A	XP_011531988.1:p.Arg2200=
XM_011533687.2:c.6589C>A	XP_011531989.1:p.Arg2197=
XM_011533688.2:c.6562C>A	XP_011531990.1:p.Arg2188=
XM_011533690.2:c.6634C>A	XP_011531992.1:p.Arg2212=
XM_017006357.2:c.6631C>A	XP_016861846.1:p.Arg2211=
NM_001099952.3:c.6487C>A	NP_001093422.2:p.Arg2163=
NM_002222.6:c.6442C>A	NP_002213.5:p.Arg2148=
NM_001099952.4:c.6487C>A	NP_001093422.2:p.Arg2163=
NM_001168272.2:c.6586C>A	NP_001161744.1:p.Arg2196=
NM_001378452.1:c.6631C>A MANE Select	NP_001365381.1:p.Arg2211=
NM_002222.7:c.6442C>A	NP_002213.5:p.Arg2148=