Canonical Allele Identifier: CA2023540522

Gene: ITPR2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.26613072C= , CM000674.2:g.26613072C=	GRCh38
NC_000012.11:g.26766005C= , CM000674.1:g.26766005C=	GRCh37
NC_000012.10:g.26657272C=	NCBI36
NG_042142.1:g.225127G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000381340.8:c.3462+8051G= MANE Select	ENSP00000370744.3:n.3462+8051G=
ENST00000381340.7:c.3462+8051G=	ENSP00000370744.3:n.3462+8051G=
NM_002223.2:c.3462+8051G=	NP_002214.2:n.3462+8051G=
NM_002223.3:c.3462+8051G=	NP_002214.2:n.3462+8051G=
XM_011520645.1:c.2910+8051G=	XP_011518947.1:n.2910+8051G=
XM_011520646.1:c.2529+8051G=	XP_011518948.1:n.2529+8051G=
XR_931288.1:n.3878+8051G=
XM_017019266.1:c.3522+8051G=	XP_016874755.1:n.3522+8051G=
XM_017019267.1:c.3456+8051G=	XP_016874756.1:n.3456+8051G=
XM_017019269.2:c.3522+8051G=	XP_016874758.1:n.3522+8051G=
XR_001748686.2:n.3938+8051G=
XR_001748687.1:n.3938+8051G=
NM_002223.4:c.3462+8051G= MANE Select	NP_002214.2:n.3462+8051G=