Canonical Allele Identifier: CA351640556

Gene: ITPR1

Linked Data

• MyVariant Identifiers: chr3:g.4829691T>A (hg19) ; chr3:g.4788007T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.4788007T>A , CM000665.2:g.4788007T>A	GRCh38
NC_000003.11:g.4829691T>A , CM000665.1:g.4829691T>A	GRCh37
NC_000003.10:g.4804691T>A	NCBI36
NG_016144.1:g.299660T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302640.13:c.6687T>A	ENSP00000306253.9:n.6687T>A
ENST00000354582.12:c.6652T>A	ENSP00000346595.8:p.Phe2218Ile
ENST00000443694.5:c.6631T>A	ENSP00000401671.2:p.Phe2211Ile
ENST00000354582.11:c.6652T>A	ENSP00000346595.8:p.Phe2218Ile
ENST00000357086.10:c.6532T>A	ENSP00000349597.4:p.Phe2178Ile
ENST00000443694.4:c.6631T>A	ENSP00000401671.2:p.Phe2211Ile
ENST00000456211.8:c.6487T>A	ENSP00000397885.2:p.Phe2163Ile
ENST00000481415.2:n.568T>A
ENST00000544951.6:c.997-18096T>A	ENSP00000440564.1:n.997-18096T>A
ENST00000647708.1:c.2575T>A
ENST00000647717.1:n.4180T>A
ENST00000648016.1:c.3011T>A
ENST00000648038.1:c.4438T>A	ENSP00000497872.1:p.Phe1480Ile
ENST00000648212.1:c.3584T>A
ENST00000648266.1:c.6649T>A	ENSP00000498014.1:p.Phe2217Ile
ENST00000648309.1:c.6604T>A	ENSP00000497026.1:p.Phe2202Ile
ENST00000648390.1:c.447-58132T>A
ENST00000648431.1:c.3978T>A
ENST00000648510.1:n.510T>A
ENST00000649015.2:c.6676T>A MANE Select	ENSP00000497605.1:p.Phe2226Ile
ENST00000649144.1:n.1724T>A
ENST00000649272.1:n.238T>A
ENST00000649694.1:n.4161T>A
ENST00000650294.1:c.6634T>A	ENSP00000498056.1:p.Phe2212Ile
ENST00000302640.12:c.6631T>A	ENSP00000306253.8:p.Phe2211Ile
ENST00000354582.10:c.6676T>A	ENSP00000346595.7:p.Phe2226Ile
ENST00000357086.9:c.6532T>A	ENSP00000349597.4:p.Phe2178Ile
ENST00000443694.3:c.6631T>A	ENSP00000401671.2:p.Phe2211Ile
ENST00000456211.7:c.6487T>A	ENSP00000397885.2:p.Phe2163Ile
ENST00000544951.5:c.997-18096T>A	ENSP00000440564.1:n.997-18096T>A
NM_001099952.2:c.6532T>A	NP_001093422.2:p.Phe2178Ile
NM_001168272.1:c.6631T>A	NP_001161744.1:p.Phe2211Ile
NM_002222.5:c.6487T>A	NP_002213.5:p.Phe2163Ile
XM_005265109.2:c.6607T>A	XP_005265166.1:p.Phe2203Ile
XM_005265110.2:c.6559T>A	XP_005265167.1:p.Phe2187Ile
XM_006713131.2:c.6610T>A	XP_006713194.1:p.Phe2204Ile
XM_011533681.1:c.6679T>A	XP_011531983.1:p.Phe2227Ile
XM_011533682.1:c.6679T>A	XP_011531984.1:p.Phe2227Ile
XM_011533683.1:c.6676T>A	XP_011531985.1:p.Phe2226Ile
XM_011533684.1:c.6652T>A	XP_011531986.1:p.Phe2218Ile
XM_011533685.1:c.6646T>A	XP_011531987.1:p.Phe2216Ile
XM_011533686.1:c.6643T>A	XP_011531988.1:p.Phe2215Ile
XM_011533687.1:c.6634T>A	XP_011531989.1:p.Phe2212Ile
XM_011533688.1:c.6607T>A	XP_011531990.1:p.Phe2203Ile
XM_011533689.1:c.6568T>A	XP_011531991.1:p.Phe2190Ile
XM_011533690.1:c.6679T>A	XP_011531992.1:p.Phe2227Ile
XM_005265109.3:c.6607T>A	XP_005265166.1:p.Phe2203Ile
XM_005265110.3:c.6559T>A	XP_005265167.1:p.Phe2187Ile
XM_006713131.3:c.6610T>A	XP_006713194.1:p.Phe2204Ile
XM_011533682.3:c.6679T>A	XP_011531984.1:p.Phe2227Ile
XM_011533683.3:c.6676T>A	XP_011531985.1:p.Phe2226Ile
XM_011533684.2:c.6652T>A	XP_011531986.1:p.Phe2218Ile
XM_011533685.2:c.6646T>A	XP_011531987.1:p.Phe2216Ile
XM_011533686.2:c.6643T>A	XP_011531988.1:p.Phe2215Ile
XM_011533687.2:c.6634T>A	XP_011531989.1:p.Phe2212Ile
XM_011533688.2:c.6607T>A	XP_011531990.1:p.Phe2203Ile
XM_011533690.2:c.6679T>A	XP_011531992.1:p.Phe2227Ile
XM_017006357.2:c.6676T>A	XP_016861846.1:p.Phe2226Ile
NM_001099952.3:c.6532T>A	NP_001093422.2:p.Phe2178Ile
NM_002222.6:c.6487T>A	NP_002213.5:p.Phe2163Ile
NM_001099952.4:c.6532T>A	NP_001093422.2:p.Phe2178Ile
NM_001168272.2:c.6631T>A	NP_001161744.1:p.Phe2211Ile
NM_001378452.1:c.6676T>A MANE Select	NP_001365381.1:p.Phe2226Ile
NM_002222.7:c.6487T>A	NP_002213.5:p.Phe2163Ile