Canonical Allele Identifier: CA2023580569

Gene: ITPR2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.26759578A= , CM000674.2:g.26759578A=	GRCh38
NC_000012.11:g.26912511A= , CM000674.1:g.26912511A=	GRCh37
NC_000012.10:g.26803778A=	NCBI36
NG_042142.1:g.78621T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381340.8:c.163+30579T= MANE Select	ENSP00000370744.3:n.163+30579T=
ENST00000242737.5:c.163+30579T=	ENSP00000242737.5:n.163+30579T=
ENST00000381340.7:c.163+30579T=	ENSP00000370744.3:n.163+30579T=
ENST00000545235.1:c.93-33813T=	ENSP00000440548.1:n.93-33813T=
NM_002223.2:c.163+30579T=	NP_002214.2:n.163+30579T=
NM_002223.3:c.163+30579T=	NP_002214.2:n.163+30579T=
XR_931288.1:n.579+30579T=
XM_017019266.1:c.163+30579T=	XP_016874755.1:n.163+30579T=
XM_017019267.1:c.97+30579T=	XP_016874756.1:n.97+30579T=
XM_017019269.2:c.163+30579T=	XP_016874758.1:n.163+30579T=
XR_001748686.2:n.579+30579T=
XR_001748687.1:n.579+30579T=
NM_002223.4:c.163+30579T= MANE Select	NP_002214.2:n.163+30579T=