Canonical Allele Identifier: CA432322332

Gene: ITPR1

Linked Data

• MyVariant Identifiers: chr3:g.4829640T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.4787956T>C , CM000665.2:g.4787956T>C	GRCh38
NC_000003.11:g.4829640T>C , CM000665.1:g.4829640T>C	GRCh37
NC_000003.10:g.4804640T>C	NCBI36
NG_016144.1:g.299609T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000302640.13:c.6636T>C	ENSP00000306253.9:n.6636T>C
ENST00000354582.12:c.6601T>C	ENSP00000346595.8:p.Leu2201=
ENST00000443694.5:c.6580T>C	ENSP00000401671.2:p.Leu2194=
ENST00000354582.11:c.6601T>C	ENSP00000346595.8:p.Leu2201=
ENST00000357086.10:c.6481T>C	ENSP00000349597.4:p.Leu2161=
ENST00000443694.4:c.6580T>C	ENSP00000401671.2:p.Leu2194=
ENST00000456211.8:c.6436T>C	ENSP00000397885.2:p.Leu2146=
ENST00000481415.2:n.517T>C
ENST00000544951.6:c.997-18147T>C	ENSP00000440564.1:n.997-18147T>C
ENST00000647708.1:c.2524T>C
ENST00000647717.1:n.4129T>C
ENST00000648016.1:c.2960T>C
ENST00000648038.1:c.4387T>C	ENSP00000497872.1:p.Leu1463=
ENST00000648212.1:c.3533T>C
ENST00000648266.1:c.6598T>C	ENSP00000498014.1:p.Leu2200=
ENST00000648309.1:c.6553T>C	ENSP00000497026.1:p.Leu2185=
ENST00000648390.1:c.447-58183T>C
ENST00000648431.1:c.3927T>C
ENST00000648510.1:n.459T>C
ENST00000649015.2:c.6625T>C MANE Select	ENSP00000497605.1:p.Leu2209=
ENST00000649144.1:n.1673T>C
ENST00000649272.1:n.187T>C
ENST00000649694.1:n.4110T>C
ENST00000650294.1:c.6583T>C	ENSP00000498056.1:p.Leu2195=
ENST00000302640.12:c.6580T>C	ENSP00000306253.8:p.Leu2194=
ENST00000354582.10:c.6625T>C	ENSP00000346595.7:p.Leu2209=
ENST00000357086.9:c.6481T>C	ENSP00000349597.4:p.Leu2161=
ENST00000443694.3:c.6580T>C	ENSP00000401671.2:p.Leu2194=
ENST00000456211.7:c.6436T>C	ENSP00000397885.2:p.Leu2146=
ENST00000481415.1:n.517T>C
ENST00000544951.5:c.997-18147T>C	ENSP00000440564.1:n.997-18147T>C
NM_001099952.2:c.6481T>C	NP_001093422.2:p.Leu2161=
NM_001168272.1:c.6580T>C	NP_001161744.1:p.Leu2194=
NM_002222.5:c.6436T>C	NP_002213.5:p.Leu2146=
XM_005265109.2:c.6556T>C	XP_005265166.1:p.Leu2186=
XM_005265110.2:c.6508T>C	XP_005265167.1:p.Leu2170=
XM_006713131.2:c.6559T>C	XP_006713194.1:p.Leu2187=
XM_011533681.1:c.6628T>C	XP_011531983.1:p.Leu2210=
XM_011533682.1:c.6628T>C	XP_011531984.1:p.Leu2210=
XM_011533683.1:c.6625T>C	XP_011531985.1:p.Leu2209=
XM_011533684.1:c.6601T>C	XP_011531986.1:p.Leu2201=
XM_011533685.1:c.6595T>C	XP_011531987.1:p.Leu2199=
XM_011533686.1:c.6592T>C	XP_011531988.1:p.Leu2198=
XM_011533687.1:c.6583T>C	XP_011531989.1:p.Leu2195=
XM_011533688.1:c.6556T>C	XP_011531990.1:p.Leu2186=
XM_011533689.1:c.6517T>C	XP_011531991.1:p.Leu2173=
XM_011533690.1:c.6628T>C	XP_011531992.1:p.Leu2210=
XM_005265109.3:c.6556T>C	XP_005265166.1:p.Leu2186=
XM_005265110.3:c.6508T>C	XP_005265167.1:p.Leu2170=
XM_006713131.3:c.6559T>C	XP_006713194.1:p.Leu2187=
XM_011533682.3:c.6628T>C	XP_011531984.1:p.Leu2210=
XM_011533683.3:c.6625T>C	XP_011531985.1:p.Leu2209=
XM_011533684.2:c.6601T>C	XP_011531986.1:p.Leu2201=
XM_011533685.2:c.6595T>C	XP_011531987.1:p.Leu2199=
XM_011533686.2:c.6592T>C	XP_011531988.1:p.Leu2198=
XM_011533687.2:c.6583T>C	XP_011531989.1:p.Leu2195=
XM_011533688.2:c.6556T>C	XP_011531990.1:p.Leu2186=
XM_011533690.2:c.6628T>C	XP_011531992.1:p.Leu2210=
XM_017006357.2:c.6625T>C	XP_016861846.1:p.Leu2209=
NM_001099952.3:c.6481T>C	NP_001093422.2:p.Leu2161=
NM_002222.6:c.6436T>C	NP_002213.5:p.Leu2146=
NM_001099952.4:c.6481T>C	NP_001093422.2:p.Leu2161=
NM_001168272.2:c.6580T>C	NP_001161744.1:p.Leu2194=
NM_001378452.1:c.6625T>C MANE Select	NP_001365381.1:p.Leu2209=
NM_002222.7:c.6436T>C	NP_002213.5:p.Leu2146=