Canonical Allele Identifier: CA351638304

Gene: ITPR1

Linked Data

• MyVariant Identifiers: chr3:g.4821268A>T (hg19) ; chr3:g.4779584A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.4779584A>T , CM000665.2:g.4779584A>T	GRCh38
NC_000003.11:g.4821268A>T , CM000665.1:g.4821268A>T	GRCh37
NC_000003.10:g.4796268A>T	NCBI36
NG_016144.1:g.291237A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302640.13:c.6337A>T	ENSP00000306253.9:n.6337A>T
ENST00000354582.12:c.6302A>T	ENSP00000346595.8:p.Glu2101Val
ENST00000443694.5:c.6281A>T	ENSP00000401671.2:p.Glu2094Val
ENST00000354582.11:c.6302A>T	ENSP00000346595.8:p.Glu2101Val
ENST00000357086.10:c.6182A>T	ENSP00000349597.4:p.Glu2061Val
ENST00000443694.4:c.6281A>T	ENSP00000401671.2:p.Glu2094Val
ENST00000456211.8:c.6137A>T	ENSP00000397885.2:p.Glu2046Val
ENST00000544951.6:c.997-26519A>T	ENSP00000440564.1:n.997-26519A>T
ENST00000647708.1:c.2225A>T
ENST00000647717.1:n.3830A>T
ENST00000648016.1:c.2661A>T
ENST00000648038.1:c.4088A>T	ENSP00000497872.1:p.Glu1363Val
ENST00000648212.1:c.3234A>T
ENST00000648266.1:c.6299A>T	ENSP00000498014.1:p.Glu2100Val
ENST00000648309.1:c.6254A>T	ENSP00000497026.1:p.Glu2085Val
ENST00000648390.1:c.447-66555A>T
ENST00000648431.1:c.3628A>T
ENST00000648510.1:n.160A>T
ENST00000649015.2:c.6326A>T MANE Select	ENSP00000497605.1:p.Glu2109Val
ENST00000649144.1:n.1374A>T
ENST00000649694.1:n.3811A>T
ENST00000650294.1:c.6284A>T	ENSP00000498056.1:p.Glu2095Val
ENST00000302640.12:c.6281A>T	ENSP00000306253.8:p.Glu2094Val
ENST00000354582.10:c.6326A>T	ENSP00000346595.7:p.Glu2109Val
ENST00000357086.9:c.6182A>T	ENSP00000349597.4:p.Glu2061Val
ENST00000443694.3:c.6281A>T	ENSP00000401671.2:p.Glu2094Val
ENST00000456211.7:c.6137A>T	ENSP00000397885.2:p.Glu2046Val
ENST00000544951.5:c.997-26519A>T	ENSP00000440564.1:n.997-26519A>T
NM_001099952.2:c.6182A>T	NP_001093422.2:p.Glu2061Val
NM_001168272.1:c.6281A>T	NP_001161744.1:p.Glu2094Val
NM_002222.5:c.6137A>T	NP_002213.5:p.Glu2046Val
XM_005265109.2:c.6257A>T	XP_005265166.1:p.Glu2086Val
XM_005265110.2:c.6209A>T	XP_005265167.1:p.Glu2070Val
XM_006713131.2:c.6260A>T	XP_006713194.1:p.Glu2087Val
XM_011533681.1:c.6329A>T	XP_011531983.1:p.Glu2110Val
XM_011533682.1:c.6329A>T	XP_011531984.1:p.Glu2110Val
XM_011533683.1:c.6326A>T	XP_011531985.1:p.Glu2109Val
XM_011533684.1:c.6302A>T	XP_011531986.1:p.Glu2101Val
XM_011533685.1:c.6296A>T	XP_011531987.1:p.Glu2099Val
XM_011533686.1:c.6293A>T	XP_011531988.1:p.Glu2098Val
XM_011533687.1:c.6284A>T	XP_011531989.1:p.Glu2095Val
XM_011533688.1:c.6257A>T	XP_011531990.1:p.Glu2086Val
XM_011533689.1:c.6218A>T	XP_011531991.1:p.Glu2073Val
XM_011533690.1:c.6329A>T	XP_011531992.1:p.Glu2110Val
XM_005265109.3:c.6257A>T	XP_005265166.1:p.Glu2086Val
XM_005265110.3:c.6209A>T	XP_005265167.1:p.Glu2070Val
XM_006713131.3:c.6260A>T	XP_006713194.1:p.Glu2087Val
XM_011533682.3:c.6329A>T	XP_011531984.1:p.Glu2110Val
XM_011533683.3:c.6326A>T	XP_011531985.1:p.Glu2109Val
XM_011533684.2:c.6302A>T	XP_011531986.1:p.Glu2101Val
XM_011533685.2:c.6296A>T	XP_011531987.1:p.Glu2099Val
XM_011533686.2:c.6293A>T	XP_011531988.1:p.Glu2098Val
XM_011533687.2:c.6284A>T	XP_011531989.1:p.Glu2095Val
XM_011533688.2:c.6257A>T	XP_011531990.1:p.Glu2086Val
XM_011533690.2:c.6329A>T	XP_011531992.1:p.Glu2110Val
XM_017006357.2:c.6326A>T	XP_016861846.1:p.Glu2109Val
NM_001099952.3:c.6182A>T	NP_001093422.2:p.Glu2061Val
NM_002222.6:c.6137A>T	NP_002213.5:p.Glu2046Val
NM_001099952.4:c.6182A>T	NP_001093422.2:p.Glu2061Val
NM_001168272.2:c.6281A>T	NP_001161744.1:p.Glu2094Val
NM_001378452.1:c.6326A>T MANE Select	NP_001365381.1:p.Glu2109Val
NM_002222.7:c.6137A>T	NP_002213.5:p.Glu2046Val