Canonical Allele Identifier: CA1620106137
Gene: ITPR3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33650250G= , CM000668.2:g.33650250G= GRCh38
NC_000006.11:g.33618027G= , CM000668.1:g.33618027G= GRCh37
NC_000006.10:g.33726005G= NCBI36
NG_027729.1:g.33872G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000605930.3:c.161-5516G= MANE Select ENSP00000475177.1:n.161-5516G=
ENST00000374316.9:c.161-5516G= ENSP00000363435.4:n.161-5516G=
ENST00000605930.2:c.161-5516G= ENSP00000475177.1:n.161-5516G=
NM_002224.3:c.161-5516G= NP_002215.2:n.161-5516G=
XM_011514576.1:c.230-5516G= XP_011512878.1:n.230-5516G=
XM_017010832.1:c.161-5516G= XP_016866321.1:n.161-5516G=
NM_002224.4:c.161-5516G= MANE Select NP_002215.2:n.161-5516G=
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