Canonical Allele Identifier: CA2560561551

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13865900_13865901insTGCTGGTGTGGTTGAGGATGGCGATGTCTGTCTGGTGTTCCTTGCTGGACTCCTGGAGGATGCCGACGGCGGCTTCAACTTCGGCTTGCTTGCGTTCGTTCTCGACGACGCACCGCATG , CM000674.2:g.13865900_13865901insTGCTGGTGTGGTTGAGGATGGCGATGTCTGTCTGGTGTTCCTTGCTGGACTCCTGGAGGATGCCGACGGCGGCTTCAACTTCGGCTTGCTTGCGTTCGTTCTCGACGACGCACCGCATG	GRCh38
NC_000012.11:g.14018834_14018835insTGCTGGTGTGGTTGAGGATGGCGATGTCTGTCTGGTGTTCCTTGCTGGACTCCTGGAGGATGCCGACGGCGGCTTCAACTTCGGCTTGCTTGCGTTCGTTCTCGACGACGCACCGCATG , CM000674.1:g.14018834_14018835insTGCTGGTGTGGTTGAGGATGGCGATGTCTGTCTGGTGTTCCTTGCTGGACTCCTGGAGGATGCCGACGGCGGCTTCAACTTCGGCTTGCTTGCGTTCGTTCTCGACGACGCACCGCATG	GRCh37
NC_000012.10:g.13910101_13910102insTGCTGGTGTGGTTGAGGATGGCGATGTCTGTCTGGTGTTCCTTGCTGGACTCCTGGAGGATGCCGACGGCGGCTTCAACTTCGGCTTGCTTGCGTTCGTTCTCGACGACGCACCGCATG	NCBI36
NG_031854.1:g.119188_119189insCATGCGGTGCGTCGTCGAGAACGAACGCAAGCAAGCCGAAGTTGAAGCCGCCGTCGGCATCCTCCAGGAGTCCAGCAAGGAACACCAGACAGACATCGCCATCCTCAACCACACCAGCA
NG_031854.2:g.121112_121113insCATGCGGTGCGTCGTCGAGAACGAACGCAAGCAAGCCGAAGTTGAAGCCGCCGTCGGCATCCTCCAGGAGTCCAGCAAGGAACACCAGACAGACATCGCCATCCTCAACCACACCAGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.308_309insCATGCGGTGCGTCGTCGAGAACGAACGCAAGCAAGCCGAAGTTGAAGCCGCCGTCGGCATCCTCCAGGAGTCCAGCAAGGAACACCAGACAGACATCGCCATCCTCAACCACACCAGCA MANE Select	ENSP00000477455.1:p.Asp104MetfsTer69
ENST00000630791.2:c.308_309insCATGCGGTGCGTCGTCGAGAACGAACGCAAGCAAGCCGAAGTTGAAGCCGCCGTCGGCATCCTCCAGGAGTCCAGCAAGGAACACCAGACAGACATCGCCATCCTCAACCACACCAGCA	ENSP00000486677.2:p.Asp104MetfsTer69
ENST00000609686.3:c.308_309insCATGCGGTGCGTCGTCGAGAACGAACGCAAGCAAGCCGAAGTTGAAGCCGCCGTCGGCATCCTCCAGGAGTCCAGCAAGGAACACCAGACAGACATCGCCATCCTCAACCACACCAGCA	ENSP00000477455.1:p.Asp104MetfsTer69
NM_000834.3:c.308_309insCATGCGGTGCGTCGTCGAGAACGAACGCAAGCAAGCCGAAGTTGAAGCCGCCGTCGGCATCCTCCAGGAGTCCAGCAAGGAACACCAGACAGACATCGCCATCCTCAACCACACCAGCA	NP_000825.2:p.Asp104MetfsTer69
XM_011520628.1:c.308_309insCATGCGGTGCGTCGTCGAGAACGAACGCAAGCAAGCCGAAGTTGAAGCCGCCGTCGGCATCCTCCAGGAGTCCAGCAAGGAACACCAGACAGACATCGCCATCCTCAACCACACCAGCA	XP_011518930.1:p.Asp104MetfsTer69
XM_011520629.1:c.308_309insCATGCGGTGCGTCGTCGAGAACGAACGCAAGCAAGCCGAAGTTGAAGCCGCCGTCGGCATCCTCCAGGAGTCCAGCAAGGAACACCAGACAGACATCGCCATCCTCAACCACACCAGCA	XP_011518931.1:p.Asp104MetfsTer69
XM_011520630.1:c.308_309insCATGCGGTGCGTCGTCGAGAACGAACGCAAGCAAGCCGAAGTTGAAGCCGCCGTCGGCATCCTCCAGGAGTCCAGCAAGGAACACCAGACAGACATCGCCATCCTCAACCACACCAGCA	XP_011518932.1:p.Asp104MetfsTer69
NM_000834.4:c.308_309insCATGCGGTGCGTCGTCGAGAACGAACGCAAGCAAGCCGAAGTTGAAGCCGCCGTCGGCATCCTCCAGGAGTCCAGCAAGGAACACCAGACAGACATCGCCATCCTCAACCACACCAGCA	NP_000825.2:p.Asp104MetfsTer69
XM_011520628.2:c.308_309insCATGCGGTGCGTCGTCGAGAACGAACGCAAGCAAGCCGAAGTTGAAGCCGCCGTCGGCATCCTCCAGGAGTCCAGCAAGGAACACCAGACAGACATCGCCATCCTCAACCACACCAGCA	XP_011518930.1:p.Asp104MetfsTer69
XM_011520629.2:c.308_309insCATGCGGTGCGTCGTCGAGAACGAACGCAAGCAAGCCGAAGTTGAAGCCGCCGTCGGCATCCTCCAGGAGTCCAGCAAGGAACACCAGACAGACATCGCCATCCTCAACCACACCAGCA	XP_011518931.1:p.Asp104MetfsTer69
XM_017019219.2:c.308_309insCATGCGGTGCGTCGTCGAGAACGAACGCAAGCAAGCCGAAGTTGAAGCCGCCGTCGGCATCCTCCAGGAGTCCAGCAAGGAACACCAGACAGACATCGCCATCCTCAACCACACCAGCA	XP_016874708.1:p.Asp104MetfsTer69
NM_000834.5:c.308_309insCATGCGGTGCGTCGTCGAGAACGAACGCAAGCAAGCCGAAGTTGAAGCCGCCGTCGGCATCCTCCAGGAGTCCAGCAAGGAACACCAGACAGACATCGCCATCCTCAACCACACCAGCA MANE Select	NP_000825.2:p.Asp104MetfsTer69