Canonical Allele Identifier: CA1342337411

Gene: ITPR1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.4787959G= , CM000665.2:g.4787959G=	GRCh38
NC_000003.11:g.4829643G= , CM000665.1:g.4829643G=	GRCh37
NC_000003.10:g.4804643G=	NCBI36
NG_016144.1:g.299612G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000302640.13:c.6639G=	ENSP00000306253.9:n.6639G=
ENST00000354582.12:c.6604G=	ENSP00000346595.8:p.Asp2202=
ENST00000443694.5:c.6583G=	ENSP00000401671.2:p.Asp2195=
ENST00000354582.11:c.6604G=	ENSP00000346595.8:p.Asp2202=
ENST00000357086.10:c.6484G=	ENSP00000349597.4:p.Asp2162=
ENST00000443694.4:c.6583G=	ENSP00000401671.2:p.Asp2195=
ENST00000456211.8:c.6439G=	ENSP00000397885.2:p.Asp2147=
ENST00000481415.2:n.520G=
ENST00000544951.6:c.997-18144G=	ENSP00000440564.1:n.997-18144G=
ENST00000647708.1:c.2527G=
ENST00000647717.1:n.4132G=
ENST00000648016.1:c.2963G=
ENST00000648038.1:c.4390G=	ENSP00000497872.1:p.Asp1464=
ENST00000648212.1:c.3536G=
ENST00000648266.1:c.6601G=	ENSP00000498014.1:p.Asp2201=
ENST00000648309.1:c.6556G=	ENSP00000497026.1:p.Asp2186=
ENST00000648390.1:c.447-58180G=
ENST00000648431.1:c.3930G=
ENST00000648510.1:n.462G=
ENST00000649015.2:c.6628G= MANE Select	ENSP00000497605.1:p.Asp2210=
ENST00000649144.1:n.1676G=
ENST00000649272.1:n.190G=
ENST00000649694.1:n.4113G=
ENST00000650294.1:c.6586G=	ENSP00000498056.1:p.Asp2196=
ENST00000302640.12:c.6583G=	ENSP00000306253.8:p.Asp2195=
ENST00000354582.10:c.6628G=	ENSP00000346595.7:p.Asp2210=
ENST00000357086.9:c.6484G=	ENSP00000349597.4:p.Asp2162=
ENST00000443694.3:c.6583G=	ENSP00000401671.2:p.Asp2195=
ENST00000456211.7:c.6439G=	ENSP00000397885.2:p.Asp2147=
ENST00000481415.1:n.520G=
ENST00000544951.5:c.997-18144G=	ENSP00000440564.1:n.997-18144G=
NM_001099952.2:c.6484G=	NP_001093422.2:p.Asp2162=
NM_001168272.1:c.6583G=	NP_001161744.1:p.Asp2195=
NM_002222.5:c.6439G=	NP_002213.5:p.Asp2147=
XM_005265109.2:c.6559G=	XP_005265166.1:p.Asp2187=
XM_005265110.2:c.6511G=	XP_005265167.1:p.Asp2171=
XM_006713131.2:c.6562G=	XP_006713194.1:p.Asp2188=
XM_011533681.1:c.6631G=	XP_011531983.1:p.Asp2211=
XM_011533682.1:c.6631G=	XP_011531984.1:p.Asp2211=
XM_011533683.1:c.6628G=	XP_011531985.1:p.Asp2210=
XM_011533684.1:c.6604G=	XP_011531986.1:p.Asp2202=
XM_011533685.1:c.6598G=	XP_011531987.1:p.Asp2200=
XM_011533686.1:c.6595G=	XP_011531988.1:p.Asp2199=
XM_011533687.1:c.6586G=	XP_011531989.1:p.Asp2196=
XM_011533688.1:c.6559G=	XP_011531990.1:p.Asp2187=
XM_011533689.1:c.6520G=	XP_011531991.1:p.Asp2174=
XM_011533690.1:c.6631G=	XP_011531992.1:p.Asp2211=
XM_005265109.3:c.6559G=	XP_005265166.1:p.Asp2187=
XM_005265110.3:c.6511G=	XP_005265167.1:p.Asp2171=
XM_006713131.3:c.6562G=	XP_006713194.1:p.Asp2188=
XM_011533682.3:c.6631G=	XP_011531984.1:p.Asp2211=
XM_011533683.3:c.6628G=	XP_011531985.1:p.Asp2210=
XM_011533684.2:c.6604G=	XP_011531986.1:p.Asp2202=
XM_011533685.2:c.6598G=	XP_011531987.1:p.Asp2200=
XM_011533686.2:c.6595G=	XP_011531988.1:p.Asp2199=
XM_011533687.2:c.6586G=	XP_011531989.1:p.Asp2196=
XM_011533688.2:c.6559G=	XP_011531990.1:p.Asp2187=
XM_011533690.2:c.6631G=	XP_011531992.1:p.Asp2211=
XM_017006357.2:c.6628G=	XP_016861846.1:p.Asp2210=
NM_001099952.3:c.6484G=	NP_001093422.2:p.Asp2162=
NM_002222.6:c.6439G=	NP_002213.5:p.Asp2147=
NM_001099952.4:c.6484G=	NP_001093422.2:p.Asp2162=
NM_001168272.2:c.6583G=	NP_001161744.1:p.Asp2195=
NM_001378452.1:c.6628G= MANE Select	NP_001365381.1:p.Asp2210=
NM_002222.7:c.6439G=	NP_002213.5:p.Asp2147=