Canonical Allele Identifier: CA2017463509

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13615695_13615696delinsAC , CM000674.2:g.13615695_13615696delinsAC	GRCh38
NC_000012.11:g.13768629_13768630delinsAC , CM000674.1:g.13768629_13768630delinsAC	GRCh37
NC_000012.10:g.13659896_13659897delinsAC	NCBI36
NG_031854.1:g.369393_369394delinsGT
NG_031854.2:g.371317_371318delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1329-32_1329-31delinsGT MANE Select	ENSP00000477455.1:n.1329-32_1329-31delinsGT
ENST00000630791.2:c.1329-32_1329-31delinsGT	ENSP00000486677.2:n.1329-32_1329-31delinsGT
ENST00000609686.3:c.1329-32_1329-31delinsGT	ENSP00000477455.1:n.1329-32_1329-31delinsGT
NM_000834.3:c.1329-32_1329-31delinsGT	NP_000825.2:n.1329-32_1329-31delinsGT
XM_011520628.1:c.1329-32_1329-31delinsGT	XP_011518930.1:n.1329-32_1329-31delinsGT
XM_011520629.1:c.1329-32_1329-31delinsGT	XP_011518931.1:n.1329-32_1329-31delinsGT
XM_011520630.1:c.1329-32_1329-31delinsGT	XP_011518932.1:n.1329-32_1329-31delinsGT
XR_931372.1:n.307+469_307+470delinsAC
XR_931373.1:n.447+469_447+470delinsAC
XR_931374.1:n.246+469_246+470delinsAC
NM_000834.4:c.1329-32_1329-31delinsGT	NP_000825.2:n.1329-32_1329-31delinsGT
XM_011520628.2:c.1329-32_1329-31delinsGT	XP_011518930.1:n.1329-32_1329-31delinsGT
XM_011520629.2:c.1329-32_1329-31delinsGT	XP_011518931.1:n.1329-32_1329-31delinsGT
XM_017019219.2:c.1329-32_1329-31delinsGT	XP_016874708.1:n.1329-32_1329-31delinsGT
XR_001749013.1:n.728+469_728+470delinsAC
XR_931372.2:n.444+469_444+470delinsAC
XR_931373.2:n.586+469_586+470delinsAC
NM_000834.5:c.1329-32_1329-31delinsGT MANE Select	NP_000825.2:n.1329-32_1329-31delinsGT