Canonical Allele Identifier: CA2017622192

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13962532_13962533delinsAT , CM000674.2:g.13962532_13962533delinsAT	GRCh38
NC_000012.11:g.14115466_14115467delinsAT , CM000674.1:g.14115466_14115467delinsAT	GRCh37
NC_000012.10:g.14006733_14006734delinsAT	NCBI36
NG_031854.1:g.22556_22557delinsAT
NG_031854.2:g.24480_24481delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.-19+17395_-19+17396delinsAT MANE Select	ENSP00000477455.1:n.-19+17395_-19+17396delinsAT
ENST00000630791.2:c.-19+17395_-19+17396delinsAT	ENSP00000486677.2:n.-19+17395_-19+17396delinsAT
ENST00000609686.3:c.-19+17395_-19+17396delinsAT	ENSP00000477455.1:n.-19+17395_-19+17396delinsAT
ENST00000627535.2:c.-19+17395_-19+17396delinsAT	ENSP00000486411.1:n.-19+17395_-19+17396delinsAT
ENST00000630791.1:c.-19+17395_-19+17396delinsAT	ENSP00000486677.1:n.-19+17395_-19+17396delinsAT
NM_000834.3:c.-19+17395_-19+17396delinsAT	NP_000825.2:n.-19+17395_-19+17396delinsAT
XM_011520628.1:c.-19+17395_-19+17396delinsAT	XP_011518930.1:n.-19+17395_-19+17396delinsAT
XM_011520629.1:c.-19+17395_-19+17396delinsAT	XP_011518931.1:n.-19+17395_-19+17396delinsAT
XM_011520630.1:c.-19+17395_-19+17396delinsAT	XP_011518932.1:n.-19+17395_-19+17396delinsAT
NM_000834.4:c.-19+17395_-19+17396delinsAT	NP_000825.2:n.-19+17395_-19+17396delinsAT
XM_011520628.2:c.-19+17395_-19+17396delinsAT	XP_011518930.1:n.-19+17395_-19+17396delinsAT
XM_011520629.2:c.-19+17395_-19+17396delinsAT	XP_011518931.1:n.-19+17395_-19+17396delinsAT
XM_017019219.2:c.-19+17395_-19+17396delinsAT	XP_016874708.1:n.-19+17395_-19+17396delinsAT
NM_000834.5:c.-19+17395_-19+17396delinsAT MANE Select	NP_000825.2:n.-19+17395_-19+17396delinsAT