Canonical Allele Identifier: CA2566017141

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13611643_13611644insAACCCT , CM000674.2:g.13611643_13611644insAACCCT	GRCh38
NC_000012.11:g.13764577_13764578insAACCCT , CM000674.1:g.13764577_13764578insAACCCT	GRCh37
NC_000012.10:g.13655844_13655845insAACCCT	NCBI36
NG_031854.1:g.373445_373446insAGGGTT
NG_031854.2:g.375369_375370insAGGGTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000609686.4:c.1780+81_1780+82insAGGGTT MANE Select	ENSP00000477455.1:n.1780+81_1780+82insAGG...
ENST00000609686.3:c.1780+81_1780+82insAGGGTT	ENSP00000477455.1:n.1780+81_1780+82insAGG...
NM_000834.3:c.1780+81_1780+82insAGGGTT	NP_000825.2:n.1780+81_1780+82insAGGGTT
XM_011520628.1:c.1780+81_1780+82insAGGGTT	XP_011518930.1:n.1780+81_1780+82insAGGGTT...
XM_011520629.1:c.1780+81_1780+82insAGGGTT	XP_011518931.1:n.1780+81_1780+82insAGGGTT...
XM_011520630.1:c.1780+81_1780+82insAGGGTT	XP_011518932.1:n.1780+81_1780+82insAGGGTT...
XR_931372.1:n.179-3455_179-3454insAACCCT
XR_931373.1:n.318+2886_318+2887insAACCCT
XR_931374.1:n.117+1043_117+1044insAACCCT
NM_000834.4:c.1780+81_1780+82insAGGGTT	NP_000825.2:n.1780+81_1780+82insAGGGTT
XM_011520628.2:c.1780+81_1780+82insAGGGTT	XP_011518930.1:n.1780+81_1780+82insAGGGTT...
XM_011520629.2:c.1780+81_1780+82insAGGGTT	XP_011518931.1:n.1780+81_1780+82insAGGGTT...
XM_017019219.2:c.1780+81_1780+82insAGGGTT	XP_016874708.1:n.1780+81_1780+82insAGGGTT...
XR_001749013.1:n.599+1043_599+1044insAACCCT
XR_931372.2:n.316-3455_316-3454insAACCCT
XR_931373.2:n.457+2886_457+2887insAACCCT
NM_000834.5:c.1780+81_1780+82insAGGGTT MANE Select	NP_000825.2:n.1780+81_1780+82insAGGGTT