Canonical Allele Identifier: CA2538532665

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13865899_13865900insGTCCCAGAAGCGCCGGTAGGTGCCGCCCGCCGCATAGAGCTCGGCGTGCGAGCCGGTCGCCTCGACGGCCCCGTCCACGAGTACGACGATGCGGTCAGCCCGGCGGATCGTGGACAGCCGGTGCGCGA , CM000674.2:g.13865899_13865900insGTCCCAGAAGCGCCGGTAGGTGCCGCCCGCCGCATAGAGCTCGGCGTGCGAGCCGGTCGCCTCGACGGCCCCGTCCACGAGTACGACGATGCGGTCAGCCCGGCGGATCGTGGACAGCCGGTGCGCGA	GRCh38
NC_000012.11:g.14018833_14018834insGTCCCAGAAGCGCCGGTAGGTGCCGCCCGCCGCATAGAGCTCGGCGTGCGAGCCGGTCGCCTCGACGGCCCCGTCCACGAGTACGACGATGCGGTCAGCCCGGCGGATCGTGGACAGCCGGTGCGCGA , CM000674.1:g.14018833_14018834insGTCCCAGAAGCGCCGGTAGGTGCCGCCCGCCGCATAGAGCTCGGCGTGCGAGCCGGTCGCCTCGACGGCCCCGTCCACGAGTACGACGATGCGGTCAGCCCGGCGGATCGTGGACAGCCGGTGCGCGA	GRCh37
NC_000012.10:g.13910100_13910101insGTCCCAGAAGCGCCGGTAGGTGCCGCCCGCCGCATAGAGCTCGGCGTGCGAGCCGGTCGCCTCGACGGCCCCGTCCACGAGTACGACGATGCGGTCAGCCCGGCGGATCGTGGACAGCCGGTGCGCGA	NCBI36
NG_031854.1:g.119189_119190insTCGCGCACCGGCTGTCCACGATCCGCCGGGCTGACCGCATCGTCGTACTCGTGGACGGGGCCGTCGAGGCGACCGGCTCGCACGCCGAGCTCTATGCGGCGGGCGGCACCTACCGGCGCTTCTGGGAC
NG_031854.2:g.121113_121114insTCGCGCACCGGCTGTCCACGATCCGCCGGGCTGACCGCATCGTCGTACTCGTGGACGGGGCCGTCGAGGCGACCGGCTCGCACGCCGAGCTCTATGCGGCGGGCGGCACCTACCGGCGCTTCTGGGAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.309_310insTCGCGCACCGGCTGTCCACGATCCGCCGGGCTGACCGCATCGTCGTACTCGTGGACGGGGCCGTCGAGGCGACCGGCTCGCACGCCGAGCTCTATGCGGCGGGCGGCACCTACCGGCGCTTCTGGGAC MANE Select	ENSP00000477455.1:p.Asp104SerfsTer72
ENST00000630791.2:c.309_310insTCGCGCACCGGCTGTCCACGATCCGCCGGGCTGACCGCATCGTCGTACTCGTGGACGGGGCCGTCGAGGCGACCGGCTCGCACGCCGAGCTCTATGCGGCGGGCGGCACCTACCGGCGCTTCTGGGAC	ENSP00000486677.2:p.Asp104SerfsTer72
ENST00000609686.3:c.309_310insTCGCGCACCGGCTGTCCACGATCCGCCGGGCTGACCGCATCGTCGTACTCGTGGACGGGGCCGTCGAGGCGACCGGCTCGCACGCCGAGCTCTATGCGGCGGGCGGCACCTACCGGCGCTTCTGGGAC	ENSP00000477455.1:p.Asp104SerfsTer72
NM_000834.3:c.309_310insTCGCGCACCGGCTGTCCACGATCCGCCGGGCTGACCGCATCGTCGTACTCGTGGACGGGGCCGTCGAGGCGACCGGCTCGCACGCCGAGCTCTATGCGGCGGGCGGCACCTACCGGCGCTTCTGGGAC	NP_000825.2:p.Asp104SerfsTer72
XM_011520628.1:c.309_310insTCGCGCACCGGCTGTCCACGATCCGCCGGGCTGACCGCATCGTCGTACTCGTGGACGGGGCCGTCGAGGCGACCGGCTCGCACGCCGAGCTCTATGCGGCGGGCGGCACCTACCGGCGCTTCTGGGAC	XP_011518930.1:p.Asp104SerfsTer72
XM_011520629.1:c.309_310insTCGCGCACCGGCTGTCCACGATCCGCCGGGCTGACCGCATCGTCGTACTCGTGGACGGGGCCGTCGAGGCGACCGGCTCGCACGCCGAGCTCTATGCGGCGGGCGGCACCTACCGGCGCTTCTGGGAC	XP_011518931.1:p.Asp104SerfsTer72
XM_011520630.1:c.309_310insTCGCGCACCGGCTGTCCACGATCCGCCGGGCTGACCGCATCGTCGTACTCGTGGACGGGGCCGTCGAGGCGACCGGCTCGCACGCCGAGCTCTATGCGGCGGGCGGCACCTACCGGCGCTTCTGGGAC	XP_011518932.1:p.Asp104SerfsTer72
NM_000834.4:c.309_310insTCGCGCACCGGCTGTCCACGATCCGCCGGGCTGACCGCATCGTCGTACTCGTGGACGGGGCCGTCGAGGCGACCGGCTCGCACGCCGAGCTCTATGCGGCGGGCGGCACCTACCGGCGCTTCTGGGAC	NP_000825.2:p.Asp104SerfsTer72
XM_011520628.2:c.309_310insTCGCGCACCGGCTGTCCACGATCCGCCGGGCTGACCGCATCGTCGTACTCGTGGACGGGGCCGTCGAGGCGACCGGCTCGCACGCCGAGCTCTATGCGGCGGGCGGCACCTACCGGCGCTTCTGGGAC	XP_011518930.1:p.Asp104SerfsTer72
XM_011520629.2:c.309_310insTCGCGCACCGGCTGTCCACGATCCGCCGGGCTGACCGCATCGTCGTACTCGTGGACGGGGCCGTCGAGGCGACCGGCTCGCACGCCGAGCTCTATGCGGCGGGCGGCACCTACCGGCGCTTCTGGGAC	XP_011518931.1:p.Asp104SerfsTer72
XM_017019219.2:c.309_310insTCGCGCACCGGCTGTCCACGATCCGCCGGGCTGACCGCATCGTCGTACTCGTGGACGGGGCCGTCGAGGCGACCGGCTCGCACGCCGAGCTCTATGCGGCGGGCGGCACCTACCGGCGCTTCTGGGAC	XP_016874708.1:p.Asp104SerfsTer72
NM_000834.5:c.309_310insTCGCGCACCGGCTGTCCACGATCCGCCGGGCTGACCGCATCGTCGTACTCGTGGACGGGGCCGTCGAGGCGACCGGCTCGCACGCCGAGCTCTATGCGGCGGGCGGCACCTACCGGCGCTTCTGGGAC MANE Select	NP_000825.2:p.Asp104SerfsTer72