Canonical Allele Identifier: CA2794601137

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13561162_13561163insTTTTTTTTC , CM000674.2:g.13561162_13561163insTTTTTTTTC	GRCh38
NC_000012.11:g.13714096_13714097insTTTTTTTTC , CM000674.1:g.13714096_13714097insTTTTTTTTC	GRCh37
NC_000012.10:g.13605363_13605364insTTTTTTTTC	NCBI36
NG_031854.1:g.423926_423927insGAAAAAAAA
NG_031854.2:g.425850_425851insGAAAAAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.*1620_*1621insGAAAAAAAA MANE Select	ENSP00000477455.1:n.*1620_*1621insGAAAAAAAA
ENST00000637214.1:c.69+47440_69+47441insGAAAAAAAA	ENSP00000489997.1:n.69+47440_69+47441insGAAAAAAAA
ENST00000609686.3:c.*1620_*1621insGAAAAAAAA	ENSP00000477455.1:n.*1620_*1621insGAAAAAAAA
XM_005253351.2:c.*1620_*1621insGAAAAAAAA	XP_005253408.1:n.*1620_*1621insGAAAAAAAA
XM_011520628.1:c.*1620_*1621insGAAAAAAAA	XP_011518930.1:n.*1620_*1621insGAAAAAAAA
XM_011520629.1:c.*1620_*1621insGAAAAAAAA	XP_011518931.1:n.*1620_*1621insGAAAAAAAA
XM_011520630.1:c.*1620_*1621insGAAAAAAAA	XP_011518932.1:n.*1620_*1621insGAAAAAAAA
NM_000834.4:c.*1620_*1621insGAAAAAAAA	NP_000825.2:n.*1620_*1621insGAAAAAAAA
XM_005253351.3:c.*1620_*1621insGAAAAAAAA	XP_005253408.1:n.*1620_*1621insGAAAAAAAA
XM_011520628.2:c.*1620_*1621insGAAAAAAAA	XP_011518930.1:n.*1620_*1621insGAAAAAAAA
XM_011520629.2:c.*1620_*1621insGAAAAAAAA	XP_011518931.1:n.*1620_*1621insGAAAAAAAA
XM_017019219.2:c.*1620_*1621insGAAAAAAAA	XP_016874708.1:n.*1620_*1621insGAAAAAAAA
NM_000834.5:c.*1620_*1621insGAAAAAAAA MANE Select	NP_000825.2:n.*1620_*1621insGAAAAAAAA