Canonical Allele Identifier: CA351638337

Gene: ITPR1

Linked Data

• MyVariant Identifiers: chr3:g.4821281C>G (hg19) ; chr3:g.4779597C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.4779597C>G , CM000665.2:g.4779597C>G	GRCh38
NC_000003.11:g.4821281C>G , CM000665.1:g.4821281C>G	GRCh37
NC_000003.10:g.4796281C>G	NCBI36
NG_016144.1:g.291250C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302640.13:c.6350C>G	ENSP00000306253.9:n.6350C>G
ENST00000354582.12:c.6315C>G	ENSP00000346595.8:p.Asp2105Glu
ENST00000443694.5:c.6294C>G	ENSP00000401671.2:p.Asp2098Glu
ENST00000354582.11:c.6315C>G	ENSP00000346595.8:p.Asp2105Glu
ENST00000357086.10:c.6195C>G	ENSP00000349597.4:p.Asp2065Glu
ENST00000443694.4:c.6294C>G	ENSP00000401671.2:p.Asp2098Glu
ENST00000456211.8:c.6150C>G	ENSP00000397885.2:p.Asp2050Glu
ENST00000544951.6:c.997-26506C>G	ENSP00000440564.1:n.997-26506C>G
ENST00000647708.1:c.2238C>G
ENST00000647717.1:n.3843C>G
ENST00000648016.1:c.2674C>G
ENST00000648038.1:c.4101C>G	ENSP00000497872.1:p.Asp1367Glu
ENST00000648212.1:c.3247C>G
ENST00000648266.1:c.6312C>G	ENSP00000498014.1:p.Asp2104Glu
ENST00000648309.1:c.6267C>G	ENSP00000497026.1:p.Asp2089Glu
ENST00000648390.1:c.447-66542C>G
ENST00000648431.1:c.3641C>G
ENST00000648510.1:n.173C>G
ENST00000649015.2:c.6339C>G MANE Select	ENSP00000497605.1:p.Asp2113Glu
ENST00000649144.1:n.1387C>G
ENST00000649694.1:n.3824C>G
ENST00000650294.1:c.6297C>G	ENSP00000498056.1:p.Asp2099Glu
ENST00000302640.12:c.6294C>G	ENSP00000306253.8:p.Asp2098Glu
ENST00000354582.10:c.6339C>G	ENSP00000346595.7:p.Asp2113Glu
ENST00000357086.9:c.6195C>G	ENSP00000349597.4:p.Asp2065Glu
ENST00000443694.3:c.6294C>G	ENSP00000401671.2:p.Asp2098Glu
ENST00000456211.7:c.6150C>G	ENSP00000397885.2:p.Asp2050Glu
ENST00000544951.5:c.997-26506C>G	ENSP00000440564.1:n.997-26506C>G
NM_001099952.2:c.6195C>G	NP_001093422.2:p.Asp2065Glu
NM_001168272.1:c.6294C>G	NP_001161744.1:p.Asp2098Glu
NM_002222.5:c.6150C>G	NP_002213.5:p.Asp2050Glu
XM_005265109.2:c.6270C>G	XP_005265166.1:p.Asp2090Glu
XM_005265110.2:c.6222C>G	XP_005265167.1:p.Asp2074Glu
XM_006713131.2:c.6273C>G	XP_006713194.1:p.Asp2091Glu
XM_011533681.1:c.6342C>G	XP_011531983.1:p.Asp2114Glu
XM_011533682.1:c.6342C>G	XP_011531984.1:p.Asp2114Glu
XM_011533683.1:c.6339C>G	XP_011531985.1:p.Asp2113Glu
XM_011533684.1:c.6315C>G	XP_011531986.1:p.Asp2105Glu
XM_011533685.1:c.6309C>G	XP_011531987.1:p.Asp2103Glu
XM_011533686.1:c.6306C>G	XP_011531988.1:p.Asp2102Glu
XM_011533687.1:c.6297C>G	XP_011531989.1:p.Asp2099Glu
XM_011533688.1:c.6270C>G	XP_011531990.1:p.Asp2090Glu
XM_011533689.1:c.6231C>G	XP_011531991.1:p.Asp2077Glu
XM_011533690.1:c.6342C>G	XP_011531992.1:p.Asp2114Glu
XM_005265109.3:c.6270C>G	XP_005265166.1:p.Asp2090Glu
XM_005265110.3:c.6222C>G	XP_005265167.1:p.Asp2074Glu
XM_006713131.3:c.6273C>G	XP_006713194.1:p.Asp2091Glu
XM_011533682.3:c.6342C>G	XP_011531984.1:p.Asp2114Glu
XM_011533683.3:c.6339C>G	XP_011531985.1:p.Asp2113Glu
XM_011533684.2:c.6315C>G	XP_011531986.1:p.Asp2105Glu
XM_011533685.2:c.6309C>G	XP_011531987.1:p.Asp2103Glu
XM_011533686.2:c.6306C>G	XP_011531988.1:p.Asp2102Glu
XM_011533687.2:c.6297C>G	XP_011531989.1:p.Asp2099Glu
XM_011533688.2:c.6270C>G	XP_011531990.1:p.Asp2090Glu
XM_011533690.2:c.6342C>G	XP_011531992.1:p.Asp2114Glu
XM_017006357.2:c.6339C>G	XP_016861846.1:p.Asp2113Glu
NM_001099952.3:c.6195C>G	NP_001093422.2:p.Asp2065Glu
NM_002222.6:c.6150C>G	NP_002213.5:p.Asp2050Glu
NM_001099952.4:c.6195C>G	NP_001093422.2:p.Asp2065Glu
NM_001168272.2:c.6294C>G	NP_001161744.1:p.Asp2098Glu
NM_001378452.1:c.6339C>G MANE Select	NP_001365381.1:p.Asp2113Glu
NM_002222.7:c.6150C>G	NP_002213.5:p.Asp2050Glu