Canonical Allele Identifier: CA351638311

Gene: ITPR1

Linked Data

• MyVariant Identifiers: chr3:g.4821271G>C (hg19) ; chr3:g.4779587G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.4779587G>C , CM000665.2:g.4779587G>C	GRCh38
NC_000003.11:g.4821271G>C , CM000665.1:g.4821271G>C	GRCh37
NC_000003.10:g.4796271G>C	NCBI36
NG_016144.1:g.291240G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302640.13:c.6340G>C	ENSP00000306253.9:n.6340G>C
ENST00000354582.12:c.6305G>C	ENSP00000346595.8:p.Ser2102Thr
ENST00000443694.5:c.6284G>C	ENSP00000401671.2:p.Ser2095Thr
ENST00000354582.11:c.6305G>C	ENSP00000346595.8:p.Ser2102Thr
ENST00000357086.10:c.6185G>C	ENSP00000349597.4:p.Ser2062Thr
ENST00000443694.4:c.6284G>C	ENSP00000401671.2:p.Ser2095Thr
ENST00000456211.8:c.6140G>C	ENSP00000397885.2:p.Ser2047Thr
ENST00000544951.6:c.997-26516G>C	ENSP00000440564.1:n.997-26516G>C
ENST00000647708.1:c.2228G>C
ENST00000647717.1:n.3833G>C
ENST00000648016.1:c.2664G>C
ENST00000648038.1:c.4091G>C	ENSP00000497872.1:p.Ser1364Thr
ENST00000648212.1:c.3237G>C
ENST00000648266.1:c.6302G>C	ENSP00000498014.1:p.Ser2101Thr
ENST00000648309.1:c.6257G>C	ENSP00000497026.1:p.Ser2086Thr
ENST00000648390.1:c.447-66552G>C
ENST00000648431.1:c.3631G>C
ENST00000648510.1:n.163G>C
ENST00000649015.2:c.6329G>C MANE Select	ENSP00000497605.1:p.Ser2110Thr
ENST00000649144.1:n.1377G>C
ENST00000649694.1:n.3814G>C
ENST00000650294.1:c.6287G>C	ENSP00000498056.1:p.Ser2096Thr
ENST00000302640.12:c.6284G>C	ENSP00000306253.8:p.Ser2095Thr
ENST00000354582.10:c.6329G>C	ENSP00000346595.7:p.Ser2110Thr
ENST00000357086.9:c.6185G>C	ENSP00000349597.4:p.Ser2062Thr
ENST00000443694.3:c.6284G>C	ENSP00000401671.2:p.Ser2095Thr
ENST00000456211.7:c.6140G>C	ENSP00000397885.2:p.Ser2047Thr
ENST00000544951.5:c.997-26516G>C	ENSP00000440564.1:n.997-26516G>C
NM_001099952.2:c.6185G>C	NP_001093422.2:p.Ser2062Thr
NM_001168272.1:c.6284G>C	NP_001161744.1:p.Ser2095Thr
NM_002222.5:c.6140G>C	NP_002213.5:p.Ser2047Thr
XM_005265109.2:c.6260G>C	XP_005265166.1:p.Ser2087Thr
XM_005265110.2:c.6212G>C	XP_005265167.1:p.Ser2071Thr
XM_006713131.2:c.6263G>C	XP_006713194.1:p.Ser2088Thr
XM_011533681.1:c.6332G>C	XP_011531983.1:p.Ser2111Thr
XM_011533682.1:c.6332G>C	XP_011531984.1:p.Ser2111Thr
XM_011533683.1:c.6329G>C	XP_011531985.1:p.Ser2110Thr
XM_011533684.1:c.6305G>C	XP_011531986.1:p.Ser2102Thr
XM_011533685.1:c.6299G>C	XP_011531987.1:p.Ser2100Thr
XM_011533686.1:c.6296G>C	XP_011531988.1:p.Ser2099Thr
XM_011533687.1:c.6287G>C	XP_011531989.1:p.Ser2096Thr
XM_011533688.1:c.6260G>C	XP_011531990.1:p.Ser2087Thr
XM_011533689.1:c.6221G>C	XP_011531991.1:p.Ser2074Thr
XM_011533690.1:c.6332G>C	XP_011531992.1:p.Ser2111Thr
XM_005265109.3:c.6260G>C	XP_005265166.1:p.Ser2087Thr
XM_005265110.3:c.6212G>C	XP_005265167.1:p.Ser2071Thr
XM_006713131.3:c.6263G>C	XP_006713194.1:p.Ser2088Thr
XM_011533682.3:c.6332G>C	XP_011531984.1:p.Ser2111Thr
XM_011533683.3:c.6329G>C	XP_011531985.1:p.Ser2110Thr
XM_011533684.2:c.6305G>C	XP_011531986.1:p.Ser2102Thr
XM_011533685.2:c.6299G>C	XP_011531987.1:p.Ser2100Thr
XM_011533686.2:c.6296G>C	XP_011531988.1:p.Ser2099Thr
XM_011533687.2:c.6287G>C	XP_011531989.1:p.Ser2096Thr
XM_011533688.2:c.6260G>C	XP_011531990.1:p.Ser2087Thr
XM_011533690.2:c.6332G>C	XP_011531992.1:p.Ser2111Thr
XM_017006357.2:c.6329G>C	XP_016861846.1:p.Ser2110Thr
NM_001099952.3:c.6185G>C	NP_001093422.2:p.Ser2062Thr
NM_002222.6:c.6140G>C	NP_002213.5:p.Ser2047Thr
NM_001099952.4:c.6185G>C	NP_001093422.2:p.Ser2062Thr
NM_001168272.2:c.6284G>C	NP_001161744.1:p.Ser2095Thr
NM_001378452.1:c.6329G>C MANE Select	NP_001365381.1:p.Ser2110Thr
NM_002222.7:c.6140G>C	NP_002213.5:p.Ser2047Thr