Canonical Allele Identifier: CA1342337424

Gene: ITPR1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.4787996G= , CM000665.2:g.4787996G=	GRCh38
NC_000003.11:g.4829680G= , CM000665.1:g.4829680G=	GRCh37
NC_000003.10:g.4804680G=	NCBI36
NG_016144.1:g.299649G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302640.13:c.6676G=	ENSP00000306253.9:n.6676G=
ENST00000354582.12:c.6641G=	ENSP00000346595.8:p.Ser2214=
ENST00000443694.5:c.6620G=	ENSP00000401671.2:p.Ser2207=
ENST00000354582.11:c.6641G=	ENSP00000346595.8:p.Ser2214=
ENST00000357086.10:c.6521G=	ENSP00000349597.4:p.Ser2174=
ENST00000443694.4:c.6620G=	ENSP00000401671.2:p.Ser2207=
ENST00000456211.8:c.6476G=	ENSP00000397885.2:p.Ser2159=
ENST00000481415.2:n.557G=
ENST00000544951.6:c.997-18107G=	ENSP00000440564.1:n.997-18107G=
ENST00000647708.1:c.2564G=
ENST00000647717.1:n.4169G=
ENST00000648016.1:c.3000G=
ENST00000648038.1:c.4427G=	ENSP00000497872.1:p.Ser1476=
ENST00000648212.1:c.3573G=
ENST00000648266.1:c.6638G=	ENSP00000498014.1:p.Ser2213=
ENST00000648309.1:c.6593G=	ENSP00000497026.1:p.Ser2198=
ENST00000648390.1:c.447-58143G=
ENST00000648431.1:c.3967G=
ENST00000648510.1:n.499G=
ENST00000649015.2:c.6665G= MANE Select	ENSP00000497605.1:p.Ser2222=
ENST00000649144.1:n.1713G=
ENST00000649272.1:n.227G=
ENST00000649694.1:n.4150G=
ENST00000650294.1:c.6623G=	ENSP00000498056.1:p.Ser2208=
ENST00000302640.12:c.6620G=	ENSP00000306253.8:p.Ser2207=
ENST00000354582.10:c.6665G=	ENSP00000346595.7:p.Ser2222=
ENST00000357086.9:c.6521G=	ENSP00000349597.4:p.Ser2174=
ENST00000443694.3:c.6620G=	ENSP00000401671.2:p.Ser2207=
ENST00000456211.7:c.6476G=	ENSP00000397885.2:p.Ser2159=
ENST00000544951.5:c.997-18107G=	ENSP00000440564.1:n.997-18107G=
NM_001099952.2:c.6521G=	NP_001093422.2:p.Ser2174=
NM_001168272.1:c.6620G=	NP_001161744.1:p.Ser2207=
NM_002222.5:c.6476G=	NP_002213.5:p.Ser2159=
XM_005265109.2:c.6596G=	XP_005265166.1:p.Ser2199=
XM_005265110.2:c.6548G=	XP_005265167.1:p.Ser2183=
XM_006713131.2:c.6599G=	XP_006713194.1:p.Ser2200=
XM_011533681.1:c.6668G=	XP_011531983.1:p.Ser2223=
XM_011533682.1:c.6668G=	XP_011531984.1:p.Ser2223=
XM_011533683.1:c.6665G=	XP_011531985.1:p.Ser2222=
XM_011533684.1:c.6641G=	XP_011531986.1:p.Ser2214=
XM_011533685.1:c.6635G=	XP_011531987.1:p.Ser2212=
XM_011533686.1:c.6632G=	XP_011531988.1:p.Ser2211=
XM_011533687.1:c.6623G=	XP_011531989.1:p.Ser2208=
XM_011533688.1:c.6596G=	XP_011531990.1:p.Ser2199=
XM_011533689.1:c.6557G=	XP_011531991.1:p.Ser2186=
XM_011533690.1:c.6668G=	XP_011531992.1:p.Ser2223=
XM_005265109.3:c.6596G=	XP_005265166.1:p.Ser2199=
XM_005265110.3:c.6548G=	XP_005265167.1:p.Ser2183=
XM_006713131.3:c.6599G=	XP_006713194.1:p.Ser2200=
XM_011533682.3:c.6668G=	XP_011531984.1:p.Ser2223=
XM_011533683.3:c.6665G=	XP_011531985.1:p.Ser2222=
XM_011533684.2:c.6641G=	XP_011531986.1:p.Ser2214=
XM_011533685.2:c.6635G=	XP_011531987.1:p.Ser2212=
XM_011533686.2:c.6632G=	XP_011531988.1:p.Ser2211=
XM_011533687.2:c.6623G=	XP_011531989.1:p.Ser2208=
XM_011533688.2:c.6596G=	XP_011531990.1:p.Ser2199=
XM_011533690.2:c.6668G=	XP_011531992.1:p.Ser2223=
XM_017006357.2:c.6665G=	XP_016861846.1:p.Ser2222=
NM_001099952.3:c.6521G=	NP_001093422.2:p.Ser2174=
NM_002222.6:c.6476G=	NP_002213.5:p.Ser2159=
NM_001099952.4:c.6521G=	NP_001093422.2:p.Ser2174=
NM_001168272.2:c.6620G=	NP_001161744.1:p.Ser2207=
NM_001378452.1:c.6665G= MANE Select	NP_001365381.1:p.Ser2222=
NM_002222.7:c.6476G=	NP_002213.5:p.Ser2159=