Canonical Allele Identifier: CA2678292648

Gene: ITPR3

Linked Data

• gnomAD v4: 6-33668776-CCGCTGTGTGCCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33668777_33668788del , CM000668.2:g.33668777_33668788del	GRCh38
NC_000006.11:g.33636554_33636565del , CM000668.1:g.33636554_33636565del	GRCh37
NC_000006.10:g.33744532_33744543del	NCBI36
NG_027729.1:g.52399_52410del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000605930.3:c.2006+143_2006+154del MANE Select	ENSP00000475177.1:n.2006+143_2006+154del
ENST00000374316.9:c.2006+143_2006+154del	ENSP00000363435.4:n.2006+143_2006+154del
ENST00000605930.2:c.2006+143_2006+154del	ENSP00000475177.1:n.2006+143_2006+154del
NM_002224.3:c.2006+143_2006+154del	NP_002215.2:n.2006+143_2006+154del
XM_011514576.1:c.2075+143_2075+154del	XP_011512878.1:n.2075+143_2075+154del
XM_011514577.1:c.1823+143_1823+154del	XP_011512879.1:n.1823+143_1823+154del
XM_011514577.3:c.1823+143_1823+154del	XP_011512879.1:n.1823+143_1823+154del
XM_017010832.1:c.2006+143_2006+154del	XP_016866321.1:n.2006+143_2006+154del
NM_002224.4:c.2006+143_2006+154del MANE Select	NP_002215.2:n.2006+143_2006+154del