Canonical Allele Identifier: CA1620116662
Gene: ITPR3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33668803G= , CM000668.2:g.33668803G= GRCh38
NC_000006.11:g.33636580G= , CM000668.1:g.33636580G= GRCh37
NC_000006.10:g.33744558G= NCBI36
NG_027729.1:g.52425G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000605930.3:c.2006+169G= MANE Select ENSP00000475177.1:n.2006+169G=
ENST00000374316.9:c.2006+169G= ENSP00000363435.4:n.2006+169G=
ENST00000605930.2:c.2006+169G= ENSP00000475177.1:n.2006+169G=
NM_002224.3:c.2006+169G= NP_002215.2:n.2006+169G=
XM_011514576.1:c.2075+169G= XP_011512878.1:n.2075+169G=
XM_011514577.1:c.1823+169G= XP_011512879.1:n.1823+169G=
XM_011514577.3:c.1823+169G= XP_011512879.1:n.1823+169G=
XM_017010832.1:c.2006+169G= XP_016866321.1:n.2006+169G=
NM_002224.4:c.2006+169G= MANE Select NP_002215.2:n.2006+169G=