Canonical Allele Identifier: CA2017510027

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13719049_13719052delinsCAAG , CM000674.2:g.13719049_13719052delinsCAAG	GRCh38
NC_000012.11:g.13871983_13871986delinsCAAG , CM000674.1:g.13871983_13871986delinsCAAG	GRCh37
NC_000012.10:g.13763250_13763253delinsCAAG	NCBI36
NG_031854.1:g.266037_266040delinsCTTG
NG_031854.2:g.267961_267964delinsCTTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000609686.4:c.1010+34265_1010+34268delinsCTTG MANE Select	ENSP00000477455.1:n.1010+34265_1010+34268...
ENST00000630791.2:c.1010+34265_1010+34268delinsCTTG	ENSP00000486677.2:n.1010+34265_1010+34268...
ENST00000609686.3:c.1010+34265_1010+34268delinsCTTG	ENSP00000477455.1:n.1010+34265_1010+34268...
NM_000834.3:c.1010+34265_1010+34268delinsCTTG	NP_000825.2:n.1010+34265_1010+34268delins...
XM_011520628.1:c.1010+34265_1010+34268delinsCTTG	XP_011518930.1:n.1010+34265_1010+34268del...
XM_011520629.1:c.1010+34265_1010+34268delinsCTTG	XP_011518931.1:n.1010+34265_1010+34268del...
XM_011520630.1:c.1010+34265_1010+34268delinsCTTG	XP_011518932.1:n.1010+34265_1010+34268del...
NM_000834.4:c.1010+34265_1010+34268delinsCTTG	NP_000825.2:n.1010+34265_1010+34268delins...
XM_011520628.2:c.1010+34265_1010+34268delinsCTTG	XP_011518930.1:n.1010+34265_1010+34268del...
XM_011520629.2:c.1010+34265_1010+34268delinsCTTG	XP_011518931.1:n.1010+34265_1010+34268del...
XM_017019219.2:c.1010+34265_1010+34268delinsCTTG	XP_016874708.1:n.1010+34265_1010+34268del...
NM_000834.5:c.1010+34265_1010+34268delinsCTTG MANE Select	NP_000825.2:n.1010+34265_1010+34268delins...