Canonical Allele Identifier: CA2794602239

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13611744_13611745insTCCAGGACATGCGTCAGCGCGTGCTGAGCTGTCTGACAGACAAGGGCGTCACCGGCGCATCGTTTGGCCCGAGCGGCACG , CM000674.2:g.13611744_13611745insTCCAGGACATGCGTCAGCGCGTGCTGAGCTGTCTGACAGACAAGGGCGTCACCGGCGCATCGTTTGGCCCGAGCGGCACG	GRCh38
NC_000012.11:g.13764678_13764679insTCCAGGACATGCGTCAGCGCGTGCTGAGCTGTCTGACAGACAAGGGCGTCACCGGCGCATCGTTTGGCCCGAGCGGCACG , CM000674.1:g.13764678_13764679insTCCAGGACATGCGTCAGCGCGTGCTGAGCTGTCTGACAGACAAGGGCGTCACCGGCGCATCGTTTGGCCCGAGCGGCACG	GRCh37
NC_000012.10:g.13655945_13655946insTCCAGGACATGCGTCAGCGCGTGCTGAGCTGTCTGACAGACAAGGGCGTCACCGGCGCATCGTTTGGCCCGAGCGGCACG	NCBI36
NG_031854.1:g.373344_373345insCGTGCCGCTCGGGCCAAACGATGCGCCGGTGACGCCCTTGTCTGTCAGACAGCTCAGCACGCGCTGACGCATGTCCTGGA
NG_031854.2:g.375268_375269insCGTGCCGCTCGGGCCAAACGATGCGCCGGTGACGCCCTTGTCTGTCAGACAGCTCAGCACGCGCTGACGCATGTCCTGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1760_1761insCGTGCCGCTCGGGCCAAACGATGCGCCGGTGACGCCCTTGTCTGTCAGACAGCTCAGCACGCGCTGACGCATGTCCTGGA MANE Select	ENSP00000477455.1:p.Arg587SerfsTer23
ENST00000609686.3:c.1760_1761insCGTGCCGCTCGGGCCAAACGATGCGCCGGTGACGCCCTTGTCTGTCAGACAGCTCAGCACGCGCTGACGCATGTCCTGGA	ENSP00000477455.1:p.Arg587SerfsTer23
NM_000834.3:c.1760_1761insCGTGCCGCTCGGGCCAAACGATGCGCCGGTGACGCCCTTGTCTGTCAGACAGCTCAGCACGCGCTGACGCATGTCCTGGA	NP_000825.2:p.Arg587SerfsTer23
XM_011520628.1:c.1760_1761insCGTGCCGCTCGGGCCAAACGATGCGCCGGTGACGCCCTTGTCTGTCAGACAGCTCAGCACGCGCTGACGCATGTCCTGGA	XP_011518930.1:p.Arg587SerfsTer23
XM_011520629.1:c.1760_1761insCGTGCCGCTCGGGCCAAACGATGCGCCGGTGACGCCCTTGTCTGTCAGACAGCTCAGCACGCGCTGACGCATGTCCTGGA	XP_011518931.1:p.Arg587SerfsTer23
XM_011520630.1:c.1760_1761insCGTGCCGCTCGGGCCAAACGATGCGCCGGTGACGCCCTTGTCTGTCAGACAGCTCAGCACGCGCTGACGCATGTCCTGGA	XP_011518932.1:p.Arg587SerfsTer23
XR_931372.1:n.179-3354_179-3353insTCCAGGACATGCGTCAGCGCGTGCTGAGCTGTCTGACAGACAAGGGCGTCACCGGCGCATCGTTTGGCCCGAGCGGCACG
XR_931373.1:n.318+2987_318+2988insTCCAGGACATGCGTCAGCGCGTGCTGAGCTGTCTGACAGACAAGGGCGTCACCGGCGCATCGTTTGGCCCGAGCGGCACG
XR_931374.1:n.117+1144_117+1145insTCCAGGACATGCGTCAGCGCGTGCTGAGCTGTCTGACAGACAAGGGCGTCACCGGCGCATCGTTTGGCCCGAGCGGCACG
NM_000834.4:c.1760_1761insCGTGCCGCTCGGGCCAAACGATGCGCCGGTGACGCCCTTGTCTGTCAGACAGCTCAGCACGCGCTGACGCATGTCCTGGA	NP_000825.2:p.Arg587SerfsTer23
XM_011520628.2:c.1760_1761insCGTGCCGCTCGGGCCAAACGATGCGCCGGTGACGCCCTTGTCTGTCAGACAGCTCAGCACGCGCTGACGCATGTCCTGGA	XP_011518930.1:p.Arg587SerfsTer23
XM_011520629.2:c.1760_1761insCGTGCCGCTCGGGCCAAACGATGCGCCGGTGACGCCCTTGTCTGTCAGACAGCTCAGCACGCGCTGACGCATGTCCTGGA	XP_011518931.1:p.Arg587SerfsTer23
XM_017019219.2:c.1760_1761insCGTGCCGCTCGGGCCAAACGATGCGCCGGTGACGCCCTTGTCTGTCAGACAGCTCAGCACGCGCTGACGCATGTCCTGGA	XP_016874708.1:p.Arg587SerfsTer23
XR_001749013.1:n.599+1144_599+1145insTCCAGGACATGCGTCAGCGCGTGCTGAGCTGTCTGACAGACAAGGGCGTCACCGGCGCATCGTTTGGCCCGAGCGGCACG
XR_931372.2:n.316-3354_316-3353insTCCAGGACATGCGTCAGCGCGTGCTGAGCTGTCTGACAGACAAGGGCGTCACCGGCGCATCGTTTGGCCCGAGCGGCACG
XR_931373.2:n.457+2987_457+2988insTCCAGGACATGCGTCAGCGCGTGCTGAGCTGTCTGACAGACAAGGGCGTCACCGGCGCATCGTTTGGCCCGAGCGGCACG
NM_000834.5:c.1760_1761insCGTGCCGCTCGGGCCAAACGATGCGCCGGTGACGCCCTTGTCTGTCAGACAGCTCAGCACGCGCTGACGCATGTCCTGGA MANE Select	NP_000825.2:p.Arg587SerfsTer23