Canonical Allele Identifier: CA2741231154

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13753933_13753934insTTTGT , CM000674.2:g.13753933_13753934insTTTGT	GRCh38
NC_000012.11:g.13906867_13906868insTTTGT , CM000674.1:g.13906867_13906868insTTTGT	GRCh37
NC_000012.10:g.13798134_13798135insTTTGT	NCBI36
NG_031854.1:g.231155_231156insACAAA
NG_031854.2:g.233079_233080insACAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.412-19_412-18insACAAA MANE Select	ENSP00000477455.1:n.412-19_412-18insACAAA
ENST00000630791.2:c.412-19_412-18insACAAA	ENSP00000486677.2:n.412-19_412-18insACAAA
ENST00000609686.3:c.412-19_412-18insACAAA	ENSP00000477455.1:n.412-19_412-18insACAAA
NM_000834.3:c.412-19_412-18insACAAA	NP_000825.2:n.412-19_412-18insACAAA
XM_011520628.1:c.412-19_412-18insACAAA	XP_011518930.1:n.412-19_412-18insACAAA
XM_011520629.1:c.412-19_412-18insACAAA	XP_011518931.1:n.412-19_412-18insACAAA
XM_011520630.1:c.412-19_412-18insACAAA	XP_011518932.1:n.412-19_412-18insACAAA
NM_000834.4:c.412-19_412-18insACAAA	NP_000825.2:n.412-19_412-18insACAAA
XM_011520628.2:c.412-19_412-18insACAAA	XP_011518930.1:n.412-19_412-18insACAAA
XM_011520629.2:c.412-19_412-18insACAAA	XP_011518931.1:n.412-19_412-18insACAAA
XM_017019219.2:c.412-19_412-18insACAAA	XP_016874708.1:n.412-19_412-18insACAAA
NM_000834.5:c.412-19_412-18insACAAA MANE Select	NP_000825.2:n.412-19_412-18insACAAA