Canonical Allele Identifier: CA2017510042

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13719084_13719086delinsATC , CM000674.2:g.13719084_13719086delinsATC	GRCh38
NC_000012.11:g.13872018_13872020delinsATC , CM000674.1:g.13872018_13872020delinsATC	GRCh37
NC_000012.10:g.13763285_13763287delinsATC	NCBI36
NG_031854.1:g.266003_266005delinsGAT
NG_031854.2:g.267927_267929delinsGAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000609686.4:c.1010+34231_1010+34233delinsGAT MANE Select	ENSP00000477455.1:n.1010+34231_1010+34233delinsGAT
ENST00000630791.2:c.1010+34231_1010+34233delinsGAT	ENSP00000486677.2:n.1010+34231_1010+34233delinsGAT
ENST00000609686.3:c.1010+34231_1010+34233delinsGAT	ENSP00000477455.1:n.1010+34231_1010+34233delinsGAT
NM_000834.3:c.1010+34231_1010+34233delinsGAT	NP_000825.2:n.1010+34231_1010+34233delinsGAT
XM_011520628.1:c.1010+34231_1010+34233delinsGAT	XP_011518930.1:n.1010+34231_1010+34233delinsGAT
XM_011520629.1:c.1010+34231_1010+34233delinsGAT	XP_011518931.1:n.1010+34231_1010+34233delinsGAT
XM_011520630.1:c.1010+34231_1010+34233delinsGAT	XP_011518932.1:n.1010+34231_1010+34233delinsGAT
NM_000834.4:c.1010+34231_1010+34233delinsGAT	NP_000825.2:n.1010+34231_1010+34233delinsGAT
XM_011520628.2:c.1010+34231_1010+34233delinsGAT	XP_011518930.1:n.1010+34231_1010+34233delinsGAT
XM_011520629.2:c.1010+34231_1010+34233delinsGAT	XP_011518931.1:n.1010+34231_1010+34233delinsGAT
XM_017019219.2:c.1010+34231_1010+34233delinsGAT	XP_016874708.1:n.1010+34231_1010+34233delinsGAT
NM_000834.5:c.1010+34231_1010+34233delinsGAT MANE Select	NP_000825.2:n.1010+34231_1010+34233delinsGAT