Canonical Allele Identifier: CA2794602236

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13611743_13611744insGAA , CM000674.2:g.13611743_13611744insGAA	GRCh38
NC_000012.11:g.13764677_13764678insGAA , CM000674.1:g.13764677_13764678insGAA	GRCh37
NC_000012.10:g.13655944_13655945insGAA	NCBI36
NG_031854.1:g.373346_373347insTCT
NG_031854.2:g.375270_375271insTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1762_1763insTCT MANE Select	ENSP00000477455.1:p.Arg587_Cys588insPhe
ENST00000609686.3:c.1762_1763insTCT	ENSP00000477455.1:p.Arg587_Cys588insPhe
NM_000834.3:c.1762_1763insTCT	NP_000825.2:p.Arg587_Cys588insPhe
XM_011520628.1:c.1762_1763insTCT	XP_011518930.1:p.Arg587_Cys588insPhe
XM_011520629.1:c.1762_1763insTCT	XP_011518931.1:p.Arg587_Cys588insPhe
XM_011520630.1:c.1762_1763insTCT	XP_011518932.1:p.Arg587_Cys588insPhe
XR_931372.1:n.179-3355_179-3354insGAA
XR_931373.1:n.318+2986_318+2987insGAA
XR_931374.1:n.117+1143_117+1144insGAA
NM_000834.4:c.1762_1763insTCT	NP_000825.2:p.Arg587_Cys588insPhe
XM_011520628.2:c.1762_1763insTCT	XP_011518930.1:p.Arg587_Cys588insPhe
XM_011520629.2:c.1762_1763insTCT	XP_011518931.1:p.Arg587_Cys588insPhe
XM_017019219.2:c.1762_1763insTCT	XP_016874708.1:p.Arg587_Cys588insPhe
XR_001749013.1:n.599+1143_599+1144insGAA
XR_931372.2:n.316-3355_316-3354insGAA
XR_931373.2:n.457+2986_457+2987insGAA
NM_000834.5:c.1762_1763insTCT MANE Select	NP_000825.2:p.Arg587_Cys588insPhe