Canonical Allele Identifier: CA432323190

Gene: ITPR1

Linked Data

• MyVariant Identifiers: chr3:g.4829771T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.4788087T>C , CM000665.2:g.4788087T>C	GRCh38
NC_000003.11:g.4829771T>C , CM000665.1:g.4829771T>C	GRCh37
NC_000003.10:g.4804771T>C	NCBI36
NG_016144.1:g.299740T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302640.13:c.6767T>C	ENSP00000306253.9:n.6767T>C
ENST00000354582.12:c.6732T>C	ENSP00000346595.8:p.Phe2244=
ENST00000443694.5:c.6711T>C	ENSP00000401671.2:p.Phe2237=
ENST00000354582.11:c.6732T>C	ENSP00000346595.8:p.Phe2244=
ENST00000357086.10:c.6612T>C	ENSP00000349597.4:p.Phe2204=
ENST00000443694.4:c.6711T>C	ENSP00000401671.2:p.Phe2237=
ENST00000456211.8:c.6567T>C	ENSP00000397885.2:p.Phe2189=
ENST00000481415.2:n.648T>C
ENST00000544951.6:c.997-18016T>C	ENSP00000440564.1:n.997-18016T>C
ENST00000647708.1:c.2655T>C
ENST00000647717.1:n.4260T>C
ENST00000648016.1:c.3091T>C
ENST00000648038.1:c.4518T>C	ENSP00000497872.1:p.Phe1506=
ENST00000648212.1:c.3664T>C
ENST00000648266.1:c.6729T>C	ENSP00000498014.1:p.Phe2243=
ENST00000648309.1:c.6684T>C	ENSP00000497026.1:p.Phe2228=
ENST00000648390.1:c.447-58052T>C
ENST00000648431.1:c.4058T>C
ENST00000648510.1:n.590T>C
ENST00000649015.2:c.6756T>C MANE Select	ENSP00000497605.1:p.Phe2252=
ENST00000649144.1:n.1804T>C
ENST00000649272.1:n.318T>C
ENST00000649694.1:n.4241T>C
ENST00000650294.1:c.6714T>C	ENSP00000498056.1:p.Phe2238=
ENST00000302640.12:c.6711T>C	ENSP00000306253.8:p.Phe2237=
ENST00000354582.10:c.6756T>C	ENSP00000346595.7:p.Phe2252=
ENST00000357086.9:c.6612T>C	ENSP00000349597.4:p.Phe2204=
ENST00000443694.3:c.6711T>C	ENSP00000401671.2:p.Phe2237=
ENST00000456211.7:c.6567T>C	ENSP00000397885.2:p.Phe2189=
ENST00000544951.5:c.997-18016T>C	ENSP00000440564.1:n.997-18016T>C
NM_001099952.2:c.6612T>C	NP_001093422.2:p.Phe2204=
NM_001168272.1:c.6711T>C	NP_001161744.1:p.Phe2237=
NM_002222.5:c.6567T>C	NP_002213.5:p.Phe2189=
XM_005265109.2:c.6687T>C	XP_005265166.1:p.Phe2229=
XM_005265110.2:c.6639T>C	XP_005265167.1:p.Phe2213=
XM_006713131.2:c.6690T>C	XP_006713194.1:p.Phe2230=
XM_011533681.1:c.6759T>C	XP_011531983.1:p.Phe2253=
XM_011533682.1:c.6759T>C	XP_011531984.1:p.Phe2253=
XM_011533683.1:c.6756T>C	XP_011531985.1:p.Phe2252=
XM_011533684.1:c.6732T>C	XP_011531986.1:p.Phe2244=
XM_011533685.1:c.6726T>C	XP_011531987.1:p.Phe2242=
XM_011533686.1:c.6723T>C	XP_011531988.1:p.Phe2241=
XM_011533687.1:c.6714T>C	XP_011531989.1:p.Phe2238=
XM_011533688.1:c.6687T>C	XP_011531990.1:p.Phe2229=
XM_011533689.1:c.6648T>C	XP_011531991.1:p.Phe2216=
XM_011533690.1:c.6759T>C	XP_011531992.1:p.Phe2253=
XM_005265109.3:c.6687T>C	XP_005265166.1:p.Phe2229=
XM_005265110.3:c.6639T>C	XP_005265167.1:p.Phe2213=
XM_006713131.3:c.6690T>C	XP_006713194.1:p.Phe2230=
XM_011533682.3:c.6759T>C	XP_011531984.1:p.Phe2253=
XM_011533683.3:c.6756T>C	XP_011531985.1:p.Phe2252=
XM_011533684.2:c.6732T>C	XP_011531986.1:p.Phe2244=
XM_011533685.2:c.6726T>C	XP_011531987.1:p.Phe2242=
XM_011533686.2:c.6723T>C	XP_011531988.1:p.Phe2241=
XM_011533687.2:c.6714T>C	XP_011531989.1:p.Phe2238=
XM_011533688.2:c.6687T>C	XP_011531990.1:p.Phe2229=
XM_011533690.2:c.6759T>C	XP_011531992.1:p.Phe2253=
XM_017006357.2:c.6756T>C	XP_016861846.1:p.Phe2252=
NM_001099952.3:c.6612T>C	NP_001093422.2:p.Phe2204=
NM_002222.6:c.6567T>C	NP_002213.5:p.Phe2189=
NM_001099952.4:c.6612T>C	NP_001093422.2:p.Phe2204=
NM_001168272.2:c.6711T>C	NP_001161744.1:p.Phe2237=
NM_001378452.1:c.6756T>C MANE Select	NP_001365381.1:p.Phe2252=
NM_002222.7:c.6567T>C	NP_002213.5:p.Phe2189=