Canonical Allele Identifier: CA2017450722

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13611772_13611778delinsTCAAAGA , CM000674.2:g.13611772_13611778delinsTCAAAGA	GRCh38
NC_000012.11:g.13764706_13764712delinsTCAAAGA , CM000674.1:g.13764706_13764712delinsTCAAAGA	GRCh37
NC_000012.10:g.13655973_13655979delinsTCAAAGA	NCBI36
NG_031854.1:g.373311_373317delinsTCTTTGA
NG_031854.2:g.375235_375241delinsTCTTTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1727_1733delinsTCTTTGA MANE Select	ENSP00000477455.1:p.Val576=
ENST00000609686.3:c.1727_1733delinsTCTTTGA	ENSP00000477455.1:p.Val576=
NM_000834.3:c.1727_1733delinsTCTTTGA	NP_000825.2:p.Val576=
XM_011520628.1:c.1727_1733delinsTCTTTGA	XP_011518930.1:p.Val576=
XM_011520629.1:c.1727_1733delinsTCTTTGA	XP_011518931.1:p.Val576=
XM_011520630.1:c.1727_1733delinsTCTTTGA	XP_011518932.1:p.Val576=
XR_931372.1:n.179-3326_179-3320delinsTCAAAGA
XR_931373.1:n.318+3015_318+3021delinsTCAAAGA
XR_931374.1:n.117+1172_117+1178delinsTCAAAGA
NM_000834.4:c.1727_1733delinsTCTTTGA	NP_000825.2:p.Val576=
XM_011520628.2:c.1727_1733delinsTCTTTGA	XP_011518930.1:p.Val576=
XM_011520629.2:c.1727_1733delinsTCTTTGA	XP_011518931.1:p.Val576=
XM_017019219.2:c.1727_1733delinsTCTTTGA	XP_016874708.1:p.Val576=
XR_001749013.1:n.599+1172_599+1178delinsTCAAAGA
XR_931372.2:n.316-3326_316-3320delinsTCAAAGA
XR_931373.2:n.457+3015_457+3021delinsTCAAAGA
NM_000834.5:c.1727_1733delinsTCTTTGA MANE Select	NP_000825.2:p.Val576=