Canonical Allele Identifier: CA1620106213
Gene: ITPR3 HGNC NCBI

Linked Data

dbSNP Id: rs1764160378

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33650437_33650449del , CM000668.2:g.33650437_33650449del GRCh38
NC_000006.11:g.33618214_33618226del , CM000668.1:g.33618214_33618226del GRCh37
NC_000006.10:g.33726192_33726204del NCBI36
NG_027729.1:g.34059_34071del

Transcript Alleles

HGVS Amino-acid change
ENST00000605930.3:c.161-5329_161-5317del MANE Select ENSP00000475177.1:n.161-5329_161-5317del
ENST00000374316.9:c.161-5329_161-5317del ENSP00000363435.4:n.161-5329_161-5317del
ENST00000605930.2:c.161-5329_161-5317del ENSP00000475177.1:n.161-5329_161-5317del
NM_002224.3:c.161-5329_161-5317del NP_002215.2:n.161-5329_161-5317del
XM_011514576.1:c.230-5329_230-5317del XP_011512878.1:n.230-5329_230-5317del
XM_017010832.1:c.161-5329_161-5317del XP_016866321.1:n.161-5329_161-5317del
NM_002224.4:c.161-5329_161-5317del MANE Select NP_002215.2:n.161-5329_161-5317del