Canonical Allele Identifier: CA2017526016

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13753928_13753929delinsCA , CM000674.2:g.13753928_13753929delinsCA	GRCh38
NC_000012.11:g.13906862_13906863delinsCA , CM000674.1:g.13906862_13906863delinsCA	GRCh37
NC_000012.10:g.13798129_13798130delinsCA	NCBI36
NG_031854.1:g.231160_231161delinsTG
NG_031854.2:g.233084_233085delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.412-14_412-13delinsTG MANE Select	ENSP00000477455.1:n.412-14_412-13delinsTG
ENST00000630791.2:c.412-14_412-13delinsTG	ENSP00000486677.2:n.412-14_412-13delinsTG
ENST00000609686.3:c.412-14_412-13delinsTG	ENSP00000477455.1:n.412-14_412-13delinsTG
NM_000834.3:c.412-14_412-13delinsTG	NP_000825.2:n.412-14_412-13delinsTG
XM_011520628.1:c.412-14_412-13delinsTG	XP_011518930.1:n.412-14_412-13delinsTG
XM_011520629.1:c.412-14_412-13delinsTG	XP_011518931.1:n.412-14_412-13delinsTG
XM_011520630.1:c.412-14_412-13delinsTG	XP_011518932.1:n.412-14_412-13delinsTG
NM_000834.4:c.412-14_412-13delinsTG	NP_000825.2:n.412-14_412-13delinsTG
XM_011520628.2:c.412-14_412-13delinsTG	XP_011518930.1:n.412-14_412-13delinsTG
XM_011520629.2:c.412-14_412-13delinsTG	XP_011518931.1:n.412-14_412-13delinsTG
XM_017019219.2:c.412-14_412-13delinsTG	XP_016874708.1:n.412-14_412-13delinsTG
NM_000834.5:c.412-14_412-13delinsTG MANE Select	NP_000825.2:n.412-14_412-13delinsTG