Canonical Allele Identifier: CA1620116772
Gene: ITPR3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33669092A= , CM000668.2:g.33669092A= GRCh38
NC_000006.11:g.33636869A= , CM000668.1:g.33636869A= GRCh37
NC_000006.10:g.33744847A= NCBI36
NG_027729.1:g.52714A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000605930.3:c.2125A= MANE Select ENSP00000475177.1:p.Arg709=
ENST00000374316.9:c.2125A= ENSP00000363435.4:p.Arg709=
ENST00000605930.2:c.2125A= ENSP00000475177.1:p.Arg709=
NM_002224.3:c.2125A= NP_002215.2:p.Arg709=
XM_011514576.1:c.2194A= XP_011512878.1:p.Arg732=
XM_011514577.1:c.1942A= XP_011512879.1:p.Arg648=
XM_011514577.3:c.1942A= XP_011512879.1:p.Arg648=
XM_017010832.1:c.2125A= XP_016866321.1:p.Arg709=
NM_002224.4:c.2125A= MANE Select NP_002215.2:p.Arg709=