Canonical Allele Identifier: CA2023540562

Gene: ITPR2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.26613167G= , CM000674.2:g.26613167G=	GRCh38
NC_000012.11:g.26766100G= , CM000674.1:g.26766100G=	GRCh37
NC_000012.10:g.26657367G=	NCBI36
NG_042142.1:g.225032C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381340.8:c.3462+7956C= MANE Select	ENSP00000370744.3:n.3462+7956C=
ENST00000381340.7:c.3462+7956C=	ENSP00000370744.3:n.3462+7956C=
NM_002223.2:c.3462+7956C=	NP_002214.2:n.3462+7956C=
NM_002223.3:c.3462+7956C=	NP_002214.2:n.3462+7956C=
XM_011520645.1:c.2910+7956C=	XP_011518947.1:n.2910+7956C=
XM_011520646.1:c.2529+7956C=	XP_011518948.1:n.2529+7956C=
XR_931288.1:n.3878+7956C=
XM_017019266.1:c.3522+7956C=	XP_016874755.1:n.3522+7956C=
XM_017019267.1:c.3456+7956C=	XP_016874756.1:n.3456+7956C=
XM_017019269.2:c.3522+7956C=	XP_016874758.1:n.3522+7956C=
XR_001748686.2:n.3938+7956C=
XR_001748687.1:n.3938+7956C=
NM_002223.4:c.3462+7956C= MANE Select	NP_002214.2:n.3462+7956C=