Canonical Allele Identifier: CA1620106155
Gene: ITPR3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33650287G= , CM000668.2:g.33650287G= GRCh38
NC_000006.11:g.33618064G= , CM000668.1:g.33618064G= GRCh37
NC_000006.10:g.33726042G= NCBI36
NG_027729.1:g.33909G=

Transcript Alleles

HGVS Amino-acid change
ENST00000605930.3:c.161-5479G= MANE Select ENSP00000475177.1:n.161-5479G=
ENST00000374316.9:c.161-5479G= ENSP00000363435.4:n.161-5479G=
ENST00000605930.2:c.161-5479G= ENSP00000475177.1:n.161-5479G=
NM_002224.3:c.161-5479G= NP_002215.2:n.161-5479G=
XM_011514576.1:c.230-5479G= XP_011512878.1:n.230-5479G=
XM_017010832.1:c.161-5479G= XP_016866321.1:n.161-5479G=
NM_002224.4:c.161-5479G= MANE Select NP_002215.2:n.161-5479G=