Canonical Allele Identifier: CA2017437155

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13561449_13561453delinsACTGT , CM000674.2:g.13561449_13561453delinsACTGT	GRCh38
NC_000012.11:g.13714383_13714387delinsACTGT , CM000674.1:g.13714383_13714387delinsACTGT	GRCh37
NC_000012.10:g.13605650_13605654delinsACTGT	NCBI36
NG_031854.1:g.423636_423640delinsACAGT
NG_031854.2:g.425560_425564delinsACAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.*1330_*1334delinsACAGT MANE Select	ENSP00000477455.1:n.*1330_*1334delinsACAGT
ENST00000637214.1:c.69+47150_69+47154delinsACAGT	ENSP00000489997.1:n.69+47150_69+47154delinsACAGT
ENST00000609686.3:c.*1330_*1334delinsACAGT	ENSP00000477455.1:n.*1330_*1334delinsACAGT
XM_005253351.2:c.*1330_*1334delinsACAGT	XP_005253408.1:n.*1330_*1334delinsACAGT
XM_011520628.1:c.*1330_*1334delinsACAGT	XP_011518930.1:n.*1330_*1334delinsACAGT
XM_011520629.1:c.*1330_*1334delinsACAGT	XP_011518931.1:n.*1330_*1334delinsACAGT
XM_011520630.1:c.*1330_*1334delinsACAGT	XP_011518932.1:n.*1330_*1334delinsACAGT
NM_000834.4:c.*1330_*1334delinsACAGT	NP_000825.2:n.*1330_*1334delinsACAGT
XM_005253351.3:c.*1330_*1334delinsACAGT	XP_005253408.1:n.*1330_*1334delinsACAGT
XM_011520628.2:c.*1330_*1334delinsACAGT	XP_011518930.1:n.*1330_*1334delinsACAGT
XM_011520629.2:c.*1330_*1334delinsACAGT	XP_011518931.1:n.*1330_*1334delinsACAGT
XM_017019219.2:c.*1330_*1334delinsACAGT	XP_016874708.1:n.*1330_*1334delinsACAGT
NM_000834.5:c.*1330_*1334delinsACAGT MANE Select	NP_000825.2:n.*1330_*1334delinsACAGT