Canonical Allele Identifier: CA2023461271
Community Standard Title: NM_002223.4(ITPR2):c.4631-6297G=
Gene: ITPR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.26568249C= , CM000674.2:g.26568249C= GRCh38
NC_000012.11:g.26721182C= , CM000674.1:g.26721182C= GRCh37
NC_000012.10:g.26612449C= NCBI36
NG_042142.1:g.269950G=

Transcript Alleles

HGVS Amino-acid Change
NM_002223.4:c.4631-6297G= MANE Select NP_002214.2:n.4631-6297G=
ENST00000381340.8:c.4631-6297G= MANE Select ENSP00000370744.3:n.4631-6297G=
NM_002223.2:c.4631-6297G= NP_002214.2:n.4631-6297G=
NM_002223.3:c.4631-6297G= NP_002214.2:n.4631-6297G=
ENST00000381340.7:c.4631-6297G= ENSP00000370744.3:n.4631-6297G=
XM_011520645.1:c.4079-6297G= XP_011518947.1:n.4079-6297G=
XM_011520646.1:c.3698-6297G= XP_011518948.1:n.3698-6297G=
XM_017019266.1:c.4691-6297G= XP_016874755.1:n.4691-6297G=
XM_017019267.1:c.4625-6297G= XP_016874756.1:n.4625-6297G=
XM_017019269.2:c.4691-6297G= XP_016874758.1:n.4691-6297G=
XR_001748686.2:n.5107-6297G=
XR_001748687.1:n.5107-6297G=
XR_931288.1:n.5047-6297G=