Canonical Allele Identifier: CA351640629

Gene: ITPR1

Linked Data

• gnomAD v4: 3-4788040-T-C
• MyVariant Identifiers: chr3:g.4829724T>C (hg19) ; chr3:g.4788040T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.4788040T>C , CM000665.2:g.4788040T>C	GRCh38
NC_000003.11:g.4829724T>C , CM000665.1:g.4829724T>C	GRCh37
NC_000003.10:g.4804724T>C	NCBI36
NG_016144.1:g.299693T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302640.13:c.6720T>C	ENSP00000306253.9:n.6720T>C
ENST00000354582.12:c.6685T>C	ENSP00000346595.8:p.Tyr2229His
ENST00000443694.5:c.6664T>C	ENSP00000401671.2:p.Tyr2222His
ENST00000354582.11:c.6685T>C	ENSP00000346595.8:p.Tyr2229His
ENST00000357086.10:c.6565T>C	ENSP00000349597.4:p.Tyr2189His
ENST00000443694.4:c.6664T>C	ENSP00000401671.2:p.Tyr2222His
ENST00000456211.8:c.6520T>C	ENSP00000397885.2:p.Tyr2174His
ENST00000481415.2:n.601T>C
ENST00000544951.6:c.997-18063T>C	ENSP00000440564.1:n.997-18063T>C
ENST00000647708.1:c.2608T>C
ENST00000647717.1:n.4213T>C
ENST00000648016.1:c.3044T>C
ENST00000648038.1:c.4471T>C	ENSP00000497872.1:p.Tyr1491His
ENST00000648212.1:c.3617T>C
ENST00000648266.1:c.6682T>C	ENSP00000498014.1:p.Tyr2228His
ENST00000648309.1:c.6637T>C	ENSP00000497026.1:p.Tyr2213His
ENST00000648390.1:c.447-58099T>C
ENST00000648431.1:c.4011T>C
ENST00000648510.1:n.543T>C
ENST00000649015.2:c.6709T>C MANE Select	ENSP00000497605.1:p.Tyr2237His
ENST00000649144.1:n.1757T>C
ENST00000649272.1:n.271T>C
ENST00000649694.1:n.4194T>C
ENST00000650294.1:c.6667T>C	ENSP00000498056.1:p.Tyr2223His
ENST00000302640.12:c.6664T>C	ENSP00000306253.8:p.Tyr2222His
ENST00000354582.10:c.6709T>C	ENSP00000346595.7:p.Tyr2237His
ENST00000357086.9:c.6565T>C	ENSP00000349597.4:p.Tyr2189His
ENST00000443694.3:c.6664T>C	ENSP00000401671.2:p.Tyr2222His
ENST00000456211.7:c.6520T>C	ENSP00000397885.2:p.Tyr2174His
ENST00000544951.5:c.997-18063T>C	ENSP00000440564.1:n.997-18063T>C
NM_001099952.2:c.6565T>C	NP_001093422.2:p.Tyr2189His
NM_001168272.1:c.6664T>C	NP_001161744.1:p.Tyr2222His
NM_002222.5:c.6520T>C	NP_002213.5:p.Tyr2174His
XM_005265109.2:c.6640T>C	XP_005265166.1:p.Tyr2214His
XM_005265110.2:c.6592T>C	XP_005265167.1:p.Tyr2198His
XM_006713131.2:c.6643T>C	XP_006713194.1:p.Tyr2215His
XM_011533681.1:c.6712T>C	XP_011531983.1:p.Tyr2238His
XM_011533682.1:c.6712T>C	XP_011531984.1:p.Tyr2238His
XM_011533683.1:c.6709T>C	XP_011531985.1:p.Tyr2237His
XM_011533684.1:c.6685T>C	XP_011531986.1:p.Tyr2229His
XM_011533685.1:c.6679T>C	XP_011531987.1:p.Tyr2227His
XM_011533686.1:c.6676T>C	XP_011531988.1:p.Tyr2226His
XM_011533687.1:c.6667T>C	XP_011531989.1:p.Tyr2223His
XM_011533688.1:c.6640T>C	XP_011531990.1:p.Tyr2214His
XM_011533689.1:c.6601T>C	XP_011531991.1:p.Tyr2201His
XM_011533690.1:c.6712T>C	XP_011531992.1:p.Tyr2238His
XM_005265109.3:c.6640T>C	XP_005265166.1:p.Tyr2214His
XM_005265110.3:c.6592T>C	XP_005265167.1:p.Tyr2198His
XM_006713131.3:c.6643T>C	XP_006713194.1:p.Tyr2215His
XM_011533682.3:c.6712T>C	XP_011531984.1:p.Tyr2238His
XM_011533683.3:c.6709T>C	XP_011531985.1:p.Tyr2237His
XM_011533684.2:c.6685T>C	XP_011531986.1:p.Tyr2229His
XM_011533685.2:c.6679T>C	XP_011531987.1:p.Tyr2227His
XM_011533686.2:c.6676T>C	XP_011531988.1:p.Tyr2226His
XM_011533687.2:c.6667T>C	XP_011531989.1:p.Tyr2223His
XM_011533688.2:c.6640T>C	XP_011531990.1:p.Tyr2214His
XM_011533690.2:c.6712T>C	XP_011531992.1:p.Tyr2238His
XM_017006357.2:c.6709T>C	XP_016861846.1:p.Tyr2237His
NM_001099952.3:c.6565T>C	NP_001093422.2:p.Tyr2189His
NM_002222.6:c.6520T>C	NP_002213.5:p.Tyr2174His
NM_001099952.4:c.6565T>C	NP_001093422.2:p.Tyr2189His
NM_001168272.2:c.6664T>C	NP_001161744.1:p.Tyr2222His
NM_001378452.1:c.6709T>C MANE Select	NP_001365381.1:p.Tyr2237His
NM_002222.7:c.6520T>C	NP_002213.5:p.Tyr2174His