Canonical Allele Identifier: CA363698031
Gene: ITPR3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33669094G>T , CM000668.2:g.33669094G>T GRCh38
NC_000006.11:g.33636871G>T , CM000668.1:g.33636871G>T GRCh37
NC_000006.10:g.33744849G>T NCBI36
NG_027729.1:g.52716G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000605930.3:c.2127G>T MANE Select ENSP00000475177.1:p.Arg709Ser
ENST00000374316.9:c.2127G>T ENSP00000363435.4:p.Arg709Ser
ENST00000605930.2:c.2127G>T ENSP00000475177.1:p.Arg709Ser
NM_002224.3:c.2127G>T NP_002215.2:p.Arg709Ser
XM_011514576.1:c.2196G>T XP_011512878.1:p.Arg732Ser
XM_011514577.1:c.1944G>T XP_011512879.1:p.Arg648Ser
XM_011514577.3:c.1944G>T XP_011512879.1:p.Arg648Ser
XM_017010832.1:c.2127G>T XP_016866321.1:p.Arg709Ser
NM_002224.4:c.2127G>T MANE Select NP_002215.2:p.Arg709Ser