Canonical Allele Identifier: CA351640430

Gene: ITPR1

Linked Data

• MyVariant Identifiers: chr3:g.4829635T>A (hg19) ; chr3:g.4787951T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.4787951T>A , CM000665.2:g.4787951T>A	GRCh38
NC_000003.11:g.4829635T>A , CM000665.1:g.4829635T>A	GRCh37
NC_000003.10:g.4804635T>A	NCBI36
NG_016144.1:g.299604T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000302640.13:c.6631T>A	ENSP00000306253.9:n.6631T>A
ENST00000354582.12:c.6596T>A	ENSP00000346595.8:p.Val2199Asp
ENST00000443694.5:c.6575T>A	ENSP00000401671.2:p.Val2192Asp
ENST00000354582.11:c.6596T>A	ENSP00000346595.8:p.Val2199Asp
ENST00000357086.10:c.6476T>A	ENSP00000349597.4:p.Val2159Asp
ENST00000443694.4:c.6575T>A	ENSP00000401671.2:p.Val2192Asp
ENST00000456211.8:c.6431T>A	ENSP00000397885.2:p.Val2144Asp
ENST00000481415.2:n.512T>A
ENST00000544951.6:c.997-18152T>A	ENSP00000440564.1:n.997-18152T>A
ENST00000647708.1:c.2519T>A
ENST00000647717.1:n.4124T>A
ENST00000648016.1:c.2955T>A
ENST00000648038.1:c.4382T>A	ENSP00000497872.1:p.Val1461Asp
ENST00000648212.1:c.3528T>A
ENST00000648266.1:c.6593T>A	ENSP00000498014.1:p.Val2198Asp
ENST00000648309.1:c.6548T>A	ENSP00000497026.1:p.Val2183Asp
ENST00000648390.1:c.447-58188T>A
ENST00000648431.1:c.3922T>A
ENST00000648510.1:n.454T>A
ENST00000649015.2:c.6620T>A MANE Select	ENSP00000497605.1:p.Val2207Asp
ENST00000649144.1:n.1668T>A
ENST00000649272.1:n.182T>A
ENST00000649694.1:n.4105T>A
ENST00000650294.1:c.6578T>A	ENSP00000498056.1:p.Val2193Asp
ENST00000302640.12:c.6575T>A	ENSP00000306253.8:p.Val2192Asp
ENST00000354582.10:c.6620T>A	ENSP00000346595.7:p.Val2207Asp
ENST00000357086.9:c.6476T>A	ENSP00000349597.4:p.Val2159Asp
ENST00000443694.3:c.6575T>A	ENSP00000401671.2:p.Val2192Asp
ENST00000456211.7:c.6431T>A	ENSP00000397885.2:p.Val2144Asp
ENST00000481415.1:n.512T>A
ENST00000544951.5:c.997-18152T>A	ENSP00000440564.1:n.997-18152T>A
NM_001099952.2:c.6476T>A	NP_001093422.2:p.Val2159Asp
NM_001168272.1:c.6575T>A	NP_001161744.1:p.Val2192Asp
NM_002222.5:c.6431T>A	NP_002213.5:p.Val2144Asp
XM_005265109.2:c.6551T>A	XP_005265166.1:p.Val2184Asp
XM_005265110.2:c.6503T>A	XP_005265167.1:p.Val2168Asp
XM_006713131.2:c.6554T>A	XP_006713194.1:p.Val2185Asp
XM_011533681.1:c.6623T>A	XP_011531983.1:p.Val2208Asp
XM_011533682.1:c.6623T>A	XP_011531984.1:p.Val2208Asp
XM_011533683.1:c.6620T>A	XP_011531985.1:p.Val2207Asp
XM_011533684.1:c.6596T>A	XP_011531986.1:p.Val2199Asp
XM_011533685.1:c.6590T>A	XP_011531987.1:p.Val2197Asp
XM_011533686.1:c.6587T>A	XP_011531988.1:p.Val2196Asp
XM_011533687.1:c.6578T>A	XP_011531989.1:p.Val2193Asp
XM_011533688.1:c.6551T>A	XP_011531990.1:p.Val2184Asp
XM_011533689.1:c.6512T>A	XP_011531991.1:p.Val2171Asp
XM_011533690.1:c.6623T>A	XP_011531992.1:p.Val2208Asp
XM_005265109.3:c.6551T>A	XP_005265166.1:p.Val2184Asp
XM_005265110.3:c.6503T>A	XP_005265167.1:p.Val2168Asp
XM_006713131.3:c.6554T>A	XP_006713194.1:p.Val2185Asp
XM_011533682.3:c.6623T>A	XP_011531984.1:p.Val2208Asp
XM_011533683.3:c.6620T>A	XP_011531985.1:p.Val2207Asp
XM_011533684.2:c.6596T>A	XP_011531986.1:p.Val2199Asp
XM_011533685.2:c.6590T>A	XP_011531987.1:p.Val2197Asp
XM_011533686.2:c.6587T>A	XP_011531988.1:p.Val2196Asp
XM_011533687.2:c.6578T>A	XP_011531989.1:p.Val2193Asp
XM_011533688.2:c.6551T>A	XP_011531990.1:p.Val2184Asp
XM_011533690.2:c.6623T>A	XP_011531992.1:p.Val2208Asp
XM_017006357.2:c.6620T>A	XP_016861846.1:p.Val2207Asp
NM_001099952.3:c.6476T>A	NP_001093422.2:p.Val2159Asp
NM_002222.6:c.6431T>A	NP_002213.5:p.Val2144Asp
NM_001099952.4:c.6476T>A	NP_001093422.2:p.Val2159Asp
NM_001168272.2:c.6575T>A	NP_001161744.1:p.Val2192Asp
NM_001378452.1:c.6620T>A MANE Select	NP_001365381.1:p.Val2207Asp
NM_002222.7:c.6431T>A	NP_002213.5:p.Val2144Asp