Canonical Allele Identifier: CA1620106157
Gene: ITPR3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33650292T= , CM000668.2:g.33650292T= GRCh38
NC_000006.11:g.33618069T= , CM000668.1:g.33618069T= GRCh37
NC_000006.10:g.33726047T= NCBI36
NG_027729.1:g.33914T=

Transcript Alleles

HGVS Amino-acid change
ENST00000605930.3:c.161-5474T= MANE Select ENSP00000475177.1:n.161-5474T=
ENST00000374316.9:c.161-5474T= ENSP00000363435.4:n.161-5474T=
ENST00000605930.2:c.161-5474T= ENSP00000475177.1:n.161-5474T=
NM_002224.3:c.161-5474T= NP_002215.2:n.161-5474T=
XM_011514576.1:c.230-5474T= XP_011512878.1:n.230-5474T=
XM_017010832.1:c.161-5474T= XP_016866321.1:n.161-5474T=
NM_002224.4:c.161-5474T= MANE Select NP_002215.2:n.161-5474T=