Canonical Allele Identifier: CA2023580675
Gene: ITPR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.26759831T= , CM000674.2:g.26759831T= GRCh38
NC_000012.11:g.26912764T= , CM000674.1:g.26912764T= GRCh37
NC_000012.10:g.26804031T= NCBI36
NG_042142.1:g.78368A=

Transcript Alleles

HGVS Amino-acid change
ENST00000381340.8:c.163+30326A= MANE Select ENSP00000370744.3:n.163+30326A=
ENST00000242737.5:c.163+30326A= ENSP00000242737.5:n.163+30326A=
ENST00000381340.7:c.163+30326A= ENSP00000370744.3:n.163+30326A=
ENST00000545235.1:c.93-34066A= ENSP00000440548.1:n.93-34066A=
NM_002223.2:c.163+30326A= NP_002214.2:n.163+30326A=
NM_002223.3:c.163+30326A= NP_002214.2:n.163+30326A=
XR_931288.1:n.579+30326A=
XM_017019266.1:c.163+30326A= XP_016874755.1:n.163+30326A=
XM_017019267.1:c.97+30326A= XP_016874756.1:n.97+30326A=
XM_017019269.2:c.163+30326A= XP_016874758.1:n.163+30326A=
XR_001748686.2:n.579+30326A=
XR_001748687.1:n.579+30326A=
NM_002223.4:c.163+30326A= MANE Select NP_002214.2:n.163+30326A=