Canonical Allele Identifier: CA2017448094

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13608932_13608936delinsCCCTT , CM000674.2:g.13608932_13608936delinsCCCTT	GRCh38
NC_000012.11:g.13761866_13761870delinsCCCTT , CM000674.1:g.13761866_13761870delinsCCCTT	GRCh37
NC_000012.10:g.13653133_13653137delinsCCCTT	NCBI36
NG_031854.1:g.376153_376157delinsAAGGG
NG_031854.2:g.378077_378081delinsAAGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1781-104_1781-100delinsAAGGG MANE Select	ENSP00000477455.1:n.1781-104_1781-100delinsAAGGG
ENST00000628166.2:n.41-104_41-100delinsAAGGG
ENST00000609686.3:c.1781-104_1781-100delinsAAGGG	ENSP00000477455.1:n.1781-104_1781-100delinsAAGGG
ENST00000628166.1:n.41-104_41-100delinsAAGGG
NM_000834.3:c.1781-104_1781-100delinsAAGGG	NP_000825.2:n.1781-104_1781-100delinsAAGGG
XM_011520628.1:c.1781-104_1781-100delinsAAGGG	XP_011518930.1:n.1781-104_1781-100delinsAAGGG
XM_011520629.1:c.1781-104_1781-100delinsAAGGG	XP_011518931.1:n.1781-104_1781-100delinsAAGGG
XM_011520630.1:c.1781-104_1781-100delinsAAGGG	XP_011518932.1:n.1781-104_1781-100delinsAAGGG
XR_931372.1:n.179-6166_179-6162delinsCCCTT
XR_931373.1:n.318+175_318+179delinsCCCTT
NM_000834.4:c.1781-104_1781-100delinsAAGGG	NP_000825.2:n.1781-104_1781-100delinsAAGGG
XM_011520628.2:c.1781-104_1781-100delinsAAGGG	XP_011518930.1:n.1781-104_1781-100delinsAAGGG
XM_011520629.2:c.1781-104_1781-100delinsAAGGG	XP_011518931.1:n.1781-104_1781-100delinsAAGGG
XM_017019219.2:c.1781-104_1781-100delinsAAGGG	XP_016874708.1:n.1781-104_1781-100delinsAAGGG
XR_001749013.1:n.457+175_457+179delinsCCCTT
XR_931372.2:n.316-6166_316-6162delinsCCCTT
XR_931373.2:n.457+175_457+179delinsCCCTT
NM_000834.5:c.1781-104_1781-100delinsAAGGG MANE Select	NP_000825.2:n.1781-104_1781-100delinsAAGGG