Canonical Allele Identifier: CA2794622736

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13865777_13865792del , CM000674.2:g.13865777_13865792del	GRCh38
NC_000012.11:g.14018711_14018726del , CM000674.1:g.14018711_14018726del	GRCh37
NC_000012.10:g.13909978_13909993del	NCBI36
NG_031854.1:g.119302_119317del
NG_031854.2:g.121226_121241del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.411+11_411+26del MANE Select	ENSP00000477455.1:n.411+11_411+26del
ENST00000630791.2:c.411+11_411+26del	ENSP00000486677.2:n.411+11_411+26del
ENST00000609686.3:c.411+11_411+26del	ENSP00000477455.1:n.411+11_411+26del
NM_000834.3:c.411+11_411+26del	NP_000825.2:n.411+11_411+26del
XM_011520628.1:c.411+11_411+26del	XP_011518930.1:n.411+11_411+26del
XM_011520629.1:c.411+11_411+26del	XP_011518931.1:n.411+11_411+26del
XM_011520630.1:c.411+11_411+26del	XP_011518932.1:n.411+11_411+26del
NM_000834.4:c.411+11_411+26del	NP_000825.2:n.411+11_411+26del
XM_011520628.2:c.411+11_411+26del	XP_011518930.1:n.411+11_411+26del
XM_011520629.2:c.411+11_411+26del	XP_011518931.1:n.411+11_411+26del
XM_017019219.2:c.411+11_411+26del	XP_016874708.1:n.411+11_411+26del
NM_000834.5:c.411+11_411+26del MANE Select	NP_000825.2:n.411+11_411+26del