Canonical Allele Identifier: CA363698101

Gene: ITPR3

Linked Data

• gnomAD v3: 6-33669110-G-T
• gnomAD v4: 6-33669110-G-T
• MyVariant Identifiers: chr6:g.33636887G>T (hg19) ; chr6:g.33669110G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33669110G>T , CM000668.2:g.33669110G>T	GRCh38
NC_000006.11:g.33636887G>T , CM000668.1:g.33636887G>T	GRCh37
NC_000006.10:g.33744865G>T	NCBI36
NG_027729.1:g.52732G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000605930.3:c.2143G>T MANE Select	ENSP00000475177.1:p.Ala715Ser
ENST00000374316.9:c.2143G>T	ENSP00000363435.4:p.Ala715Ser
ENST00000605930.2:c.2143G>T	ENSP00000475177.1:p.Ala715Ser
NM_002224.3:c.2143G>T	NP_002215.2:p.Ala715Ser
XM_011514576.1:c.2212G>T	XP_011512878.1:p.Ala738Ser
XM_011514577.1:c.1960G>T	XP_011512879.1:p.Ala654Ser
XM_011514577.3:c.1960G>T	XP_011512879.1:p.Ala654Ser
XM_017010832.1:c.2143G>T	XP_016866321.1:p.Ala715Ser
NM_002224.4:c.2143G>T MANE Select	NP_002215.2:p.Ala715Ser