Canonical Allele Identifier: CA2017463079

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13615316_13615319delinsGACC , CM000674.2:g.13615316_13615319delinsGACC	GRCh38
NC_000012.11:g.13768250_13768253delinsGACC , CM000674.1:g.13768250_13768253delinsGACC	GRCh37
NC_000012.10:g.13659517_13659520delinsGACC	NCBI36
NG_031854.1:g.369770_369773delinsGGTC
NG_031854.2:g.371694_371697delinsGGTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1501-52_1501-49delinsGGTC MANE Select	ENSP00000477455.1:n.1501-52_1501-49delinsGGTC
ENST00000609686.3:c.1501-52_1501-49delinsGGTC	ENSP00000477455.1:n.1501-52_1501-49delinsGGTC
NM_000834.3:c.1501-52_1501-49delinsGGTC	NP_000825.2:n.1501-52_1501-49delinsGGTC
XM_011520628.1:c.1501-52_1501-49delinsGGTC	XP_011518930.1:n.1501-52_1501-49delinsGGTC
XM_011520629.1:c.1501-52_1501-49delinsGGTC	XP_011518931.1:n.1501-52_1501-49delinsGGTC
XM_011520630.1:c.1501-52_1501-49delinsGGTC	XP_011518932.1:n.1501-52_1501-49delinsGGTC
XR_931372.1:n.307+90_307+93delinsGACC
XR_931373.1:n.447+90_447+93delinsGACC
XR_931374.1:n.246+90_246+93delinsGACC
NM_000834.4:c.1501-52_1501-49delinsGGTC	NP_000825.2:n.1501-52_1501-49delinsGGTC
XM_011520628.2:c.1501-52_1501-49delinsGGTC	XP_011518930.1:n.1501-52_1501-49delinsGGTC
XM_011520629.2:c.1501-52_1501-49delinsGGTC	XP_011518931.1:n.1501-52_1501-49delinsGGTC
XM_017019219.2:c.1501-52_1501-49delinsGGTC	XP_016874708.1:n.1501-52_1501-49delinsGGTC
XR_001749013.1:n.728+90_728+93delinsGACC
XR_931372.2:n.444+90_444+93delinsGACC
XR_931373.2:n.586+90_586+93delinsGACC
NM_000834.5:c.1501-52_1501-49delinsGGTC MANE Select	NP_000825.2:n.1501-52_1501-49delinsGGTC