Canonical Allele Identifier: CA2023531077
Community Standard Title: NM_002223.4(ITPR2):c.1410-895A=
Gene: ITPR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.26666946T= , CM000674.2:g.26666946T= GRCh38
NC_000012.11:g.26819879T= , CM000674.1:g.26819879T= GRCh37
NC_000012.10:g.26711146T= NCBI36
NG_042142.1:g.171253A=

Transcript Alleles

HGVS Amino-acid Change
NM_002223.4:c.1410-895A= MANE Select NP_002214.2:n.1410-895A=
ENST00000381340.8:c.1410-895A= MANE Select ENSP00000370744.3:n.1410-895A=
NM_002223.2:c.1410-895A= NP_002214.2:n.1410-895A=
NM_002223.3:c.1410-895A= NP_002214.2:n.1410-895A=
ENST00000381340.7:c.1410-895A= ENSP00000370744.3:n.1410-895A=
XM_011520645.1:c.858-895A= XP_011518947.1:n.858-895A=
XM_011520646.1:c.477-895A= XP_011518948.1:n.477-895A=
XM_017019266.1:c.1470-895A= XP_016874755.1:n.1470-895A=
XM_017019267.1:c.1404-895A= XP_016874756.1:n.1404-895A=
XM_017019269.2:c.1470-895A= XP_016874758.1:n.1470-895A=
XR_001748686.2:n.1886-895A=
XR_001748687.1:n.1886-895A=
XR_931288.1:n.1826-895A=