Canonical Allele Identifier: CA1342337429

Gene: ITPR1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.4788018G= , CM000665.2:g.4788018G=	GRCh38
NC_000003.11:g.4829702G= , CM000665.1:g.4829702G=	GRCh37
NC_000003.10:g.4804702G=	NCBI36
NG_016144.1:g.299671G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302640.13:c.6698G=	ENSP00000306253.9:n.6698G=
ENST00000354582.12:c.6663G=	ENSP00000346595.8:p.Lys2221=
ENST00000443694.5:c.6642G=	ENSP00000401671.2:p.Lys2214=
ENST00000354582.11:c.6663G=	ENSP00000346595.8:p.Lys2221=
ENST00000357086.10:c.6543G=	ENSP00000349597.4:p.Lys2181=
ENST00000443694.4:c.6642G=	ENSP00000401671.2:p.Lys2214=
ENST00000456211.8:c.6498G=	ENSP00000397885.2:p.Lys2166=
ENST00000481415.2:n.579G=
ENST00000544951.6:c.997-18085G=	ENSP00000440564.1:n.997-18085G=
ENST00000647708.1:c.2586G=
ENST00000647717.1:n.4191G=
ENST00000648016.1:c.3022G=
ENST00000648038.1:c.4449G=	ENSP00000497872.1:p.Lys1483=
ENST00000648212.1:c.3595G=
ENST00000648266.1:c.6660G=	ENSP00000498014.1:p.Lys2220=
ENST00000648309.1:c.6615G=	ENSP00000497026.1:p.Lys2205=
ENST00000648390.1:c.447-58121G=
ENST00000648431.1:c.3989G=
ENST00000648510.1:n.521G=
ENST00000649015.2:c.6687G= MANE Select	ENSP00000497605.1:p.Lys2229=
ENST00000649144.1:n.1735G=
ENST00000649272.1:n.249G=
ENST00000649694.1:n.4172G=
ENST00000650294.1:c.6645G=	ENSP00000498056.1:p.Lys2215=
ENST00000302640.12:c.6642G=	ENSP00000306253.8:p.Lys2214=
ENST00000354582.10:c.6687G=	ENSP00000346595.7:p.Lys2229=
ENST00000357086.9:c.6543G=	ENSP00000349597.4:p.Lys2181=
ENST00000443694.3:c.6642G=	ENSP00000401671.2:p.Lys2214=
ENST00000456211.7:c.6498G=	ENSP00000397885.2:p.Lys2166=
ENST00000544951.5:c.997-18085G=	ENSP00000440564.1:n.997-18085G=
NM_001099952.2:c.6543G=	NP_001093422.2:p.Lys2181=
NM_001168272.1:c.6642G=	NP_001161744.1:p.Lys2214=
NM_002222.5:c.6498G=	NP_002213.5:p.Lys2166=
XM_005265109.2:c.6618G=	XP_005265166.1:p.Lys2206=
XM_005265110.2:c.6570G=	XP_005265167.1:p.Lys2190=
XM_006713131.2:c.6621G=	XP_006713194.1:p.Lys2207=
XM_011533681.1:c.6690G=	XP_011531983.1:p.Lys2230=
XM_011533682.1:c.6690G=	XP_011531984.1:p.Lys2230=
XM_011533683.1:c.6687G=	XP_011531985.1:p.Lys2229=
XM_011533684.1:c.6663G=	XP_011531986.1:p.Lys2221=
XM_011533685.1:c.6657G=	XP_011531987.1:p.Lys2219=
XM_011533686.1:c.6654G=	XP_011531988.1:p.Lys2218=
XM_011533687.1:c.6645G=	XP_011531989.1:p.Lys2215=
XM_011533688.1:c.6618G=	XP_011531990.1:p.Lys2206=
XM_011533689.1:c.6579G=	XP_011531991.1:p.Lys2193=
XM_011533690.1:c.6690G=	XP_011531992.1:p.Lys2230=
XM_005265109.3:c.6618G=	XP_005265166.1:p.Lys2206=
XM_005265110.3:c.6570G=	XP_005265167.1:p.Lys2190=
XM_006713131.3:c.6621G=	XP_006713194.1:p.Lys2207=
XM_011533682.3:c.6690G=	XP_011531984.1:p.Lys2230=
XM_011533683.3:c.6687G=	XP_011531985.1:p.Lys2229=
XM_011533684.2:c.6663G=	XP_011531986.1:p.Lys2221=
XM_011533685.2:c.6657G=	XP_011531987.1:p.Lys2219=
XM_011533686.2:c.6654G=	XP_011531988.1:p.Lys2218=
XM_011533687.2:c.6645G=	XP_011531989.1:p.Lys2215=
XM_011533688.2:c.6618G=	XP_011531990.1:p.Lys2206=
XM_011533690.2:c.6690G=	XP_011531992.1:p.Lys2230=
XM_017006357.2:c.6687G=	XP_016861846.1:p.Lys2229=
NM_001099952.3:c.6543G=	NP_001093422.2:p.Lys2181=
NM_002222.6:c.6498G=	NP_002213.5:p.Lys2166=
NM_001099952.4:c.6543G=	NP_001093422.2:p.Lys2181=
NM_001168272.2:c.6642G=	NP_001161744.1:p.Lys2214=
NM_001378452.1:c.6687G= MANE Select	NP_001365381.1:p.Lys2229=
NM_002222.7:c.6498G=	NP_002213.5:p.Lys2166=