Canonical Allele Identifier: CA351640688

Gene: ITPR1

Linked Data

• MyVariant Identifiers: chr3:g.4829749G>T (hg19) ; chr3:g.4788065G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.4788065G>T , CM000665.2:g.4788065G>T	GRCh38
NC_000003.11:g.4829749G>T , CM000665.1:g.4829749G>T	GRCh37
NC_000003.10:g.4804749G>T	NCBI36
NG_016144.1:g.299718G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302640.13:c.6745G>T	ENSP00000306253.9:n.6745G>T
ENST00000354582.12:c.6710G>T	ENSP00000346595.8:p.Gly2237Val
ENST00000443694.5:c.6689G>T	ENSP00000401671.2:p.Gly2230Val
ENST00000354582.11:c.6710G>T	ENSP00000346595.8:p.Gly2237Val
ENST00000357086.10:c.6590G>T	ENSP00000349597.4:p.Gly2197Val
ENST00000443694.4:c.6689G>T	ENSP00000401671.2:p.Gly2230Val
ENST00000456211.8:c.6545G>T	ENSP00000397885.2:p.Gly2182Val
ENST00000481415.2:n.626G>T
ENST00000544951.6:c.997-18038G>T	ENSP00000440564.1:n.997-18038G>T
ENST00000647708.1:c.2633G>T
ENST00000647717.1:n.4238G>T
ENST00000648016.1:c.3069G>T
ENST00000648038.1:c.4496G>T	ENSP00000497872.1:p.Gly1499Val
ENST00000648212.1:c.3642G>T
ENST00000648266.1:c.6707G>T	ENSP00000498014.1:p.Gly2236Val
ENST00000648309.1:c.6662G>T	ENSP00000497026.1:p.Gly2221Val
ENST00000648390.1:c.447-58074G>T
ENST00000648431.1:c.4036G>T
ENST00000648510.1:n.568G>T
ENST00000649015.2:c.6734G>T MANE Select	ENSP00000497605.1:p.Gly2245Val
ENST00000649144.1:n.1782G>T
ENST00000649272.1:n.296G>T
ENST00000649694.1:n.4219G>T
ENST00000650294.1:c.6692G>T	ENSP00000498056.1:p.Gly2231Val
ENST00000302640.12:c.6689G>T	ENSP00000306253.8:p.Gly2230Val
ENST00000354582.10:c.6734G>T	ENSP00000346595.7:p.Gly2245Val
ENST00000357086.9:c.6590G>T	ENSP00000349597.4:p.Gly2197Val
ENST00000443694.3:c.6689G>T	ENSP00000401671.2:p.Gly2230Val
ENST00000456211.7:c.6545G>T	ENSP00000397885.2:p.Gly2182Val
ENST00000544951.5:c.997-18038G>T	ENSP00000440564.1:n.997-18038G>T
NM_001099952.2:c.6590G>T	NP_001093422.2:p.Gly2197Val
NM_001168272.1:c.6689G>T	NP_001161744.1:p.Gly2230Val
NM_002222.5:c.6545G>T	NP_002213.5:p.Gly2182Val
XM_005265109.2:c.6665G>T	XP_005265166.1:p.Gly2222Val
XM_005265110.2:c.6617G>T	XP_005265167.1:p.Gly2206Val
XM_006713131.2:c.6668G>T	XP_006713194.1:p.Gly2223Val
XM_011533681.1:c.6737G>T	XP_011531983.1:p.Gly2246Val
XM_011533682.1:c.6737G>T	XP_011531984.1:p.Gly2246Val
XM_011533683.1:c.6734G>T	XP_011531985.1:p.Gly2245Val
XM_011533684.1:c.6710G>T	XP_011531986.1:p.Gly2237Val
XM_011533685.1:c.6704G>T	XP_011531987.1:p.Gly2235Val
XM_011533686.1:c.6701G>T	XP_011531988.1:p.Gly2234Val
XM_011533687.1:c.6692G>T	XP_011531989.1:p.Gly2231Val
XM_011533688.1:c.6665G>T	XP_011531990.1:p.Gly2222Val
XM_011533689.1:c.6626G>T	XP_011531991.1:p.Gly2209Val
XM_011533690.1:c.6737G>T	XP_011531992.1:p.Gly2246Val
XM_005265109.3:c.6665G>T	XP_005265166.1:p.Gly2222Val
XM_005265110.3:c.6617G>T	XP_005265167.1:p.Gly2206Val
XM_006713131.3:c.6668G>T	XP_006713194.1:p.Gly2223Val
XM_011533682.3:c.6737G>T	XP_011531984.1:p.Gly2246Val
XM_011533683.3:c.6734G>T	XP_011531985.1:p.Gly2245Val
XM_011533684.2:c.6710G>T	XP_011531986.1:p.Gly2237Val
XM_011533685.2:c.6704G>T	XP_011531987.1:p.Gly2235Val
XM_011533686.2:c.6701G>T	XP_011531988.1:p.Gly2234Val
XM_011533687.2:c.6692G>T	XP_011531989.1:p.Gly2231Val
XM_011533688.2:c.6665G>T	XP_011531990.1:p.Gly2222Val
XM_011533690.2:c.6737G>T	XP_011531992.1:p.Gly2246Val
XM_017006357.2:c.6734G>T	XP_016861846.1:p.Gly2245Val
NM_001099952.3:c.6590G>T	NP_001093422.2:p.Gly2197Val
NM_002222.6:c.6545G>T	NP_002213.5:p.Gly2182Val
NM_001099952.4:c.6590G>T	NP_001093422.2:p.Gly2197Val
NM_001168272.2:c.6689G>T	NP_001161744.1:p.Gly2230Val
NM_001378452.1:c.6734G>T MANE Select	NP_001365381.1:p.Gly2245Val
NM_002222.7:c.6545G>T	NP_002213.5:p.Gly2182Val