Canonical Allele Identifier: CA2017463162

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13615377_13615387delinsCTTATTTGCCA , CM000674.2:g.13615377_13615387delinsCTTATTTGCCA	GRCh38
NC_000012.11:g.13768311_13768321delinsCTTATTTGCCA , CM000674.1:g.13768311_13768321delinsCTTATTTGCCA	GRCh37
NC_000012.10:g.13659578_13659588delinsCTTATTTGCCA	NCBI36
NG_031854.1:g.369702_369712delinsTGGCAAATAAG
NG_031854.2:g.371626_371636delinsTGGCAAATAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1500+106_1501-110delinsTGGCAAATAAG MANE Select	ENSP00000477455.1:n.1500+106_1501-110delinsTGGCAAATAAG
ENST00000609686.3:c.1500+106_1501-110delinsTGGCAAATAAG	ENSP00000477455.1:n.1500+106_1501-110delinsTGGCAAATAAG
NM_000834.3:c.1500+106_1501-110delinsTGGCAAATAAG	NP_000825.2:n.1500+106_1501-110delinsTGGCAAATAAG
XM_011520628.1:c.1500+106_1501-110delinsTGGCAAATAAG	XP_011518930.1:n.1500+106_1501-110delinsTGGCAAATAAG
XM_011520629.1:c.1500+106_1501-110delinsTGGCAAATAAG	XP_011518931.1:n.1500+106_1501-110delinsTGGCAAATAAG
XM_011520630.1:c.1500+106_1501-110delinsTGGCAAATAAG	XP_011518932.1:n.1500+106_1501-110delinsTGGCAAATAAG
XR_931372.1:n.307+151_307+161delinsCTTATTTGCCA
XR_931373.1:n.447+151_447+161delinsCTTATTTGCCA
XR_931374.1:n.246+151_246+161delinsCTTATTTGCCA
NM_000834.4:c.1500+106_1501-110delinsTGGCAAATAAG	NP_000825.2:n.1500+106_1501-110delinsTGGCAAATAAG
XM_011520628.2:c.1500+106_1501-110delinsTGGCAAATAAG	XP_011518930.1:n.1500+106_1501-110delinsTGGCAAATAAG
XM_011520629.2:c.1500+106_1501-110delinsTGGCAAATAAG	XP_011518931.1:n.1500+106_1501-110delinsTGGCAAATAAG
XM_017019219.2:c.1500+106_1501-110delinsTGGCAAATAAG	XP_016874708.1:n.1500+106_1501-110delinsTGGCAAATAAG
XR_001749013.1:n.728+151_728+161delinsCTTATTTGCCA
XR_931372.2:n.444+151_444+161delinsCTTATTTGCCA
XR_931373.2:n.586+151_586+161delinsCTTATTTGCCA
NM_000834.5:c.1500+106_1501-110delinsTGGCAAATAAG MANE Select	NP_000825.2:n.1500+106_1501-110delinsTGGCAAATAAG