Canonical Allele Identifier: CA2017622217

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13962596_13962597delinsGT , CM000674.2:g.13962596_13962597delinsGT	GRCh38
NC_000012.11:g.14115530_14115531delinsGT , CM000674.1:g.14115530_14115531delinsGT	GRCh37
NC_000012.10:g.14006797_14006798delinsGT	NCBI36
NG_031854.1:g.22492_22493delinsAC
NG_031854.2:g.24416_24417delinsAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000609686.4:c.-19+17331_-19+17332delinsAC MANE Select	ENSP00000477455.1:n.-19+17331_-19+17332de...
ENST00000630791.2:c.-19+17331_-19+17332delinsAC	ENSP00000486677.2:n.-19+17331_-19+17332de...
ENST00000609686.3:c.-19+17331_-19+17332delinsAC	ENSP00000477455.1:n.-19+17331_-19+17332de...
ENST00000627535.2:c.-19+17331_-19+17332delinsAC	ENSP00000486411.1:n.-19+17331_-19+17332de...
ENST00000630791.1:c.-19+17331_-19+17332delinsAC	ENSP00000486677.1:n.-19+17331_-19+17332de...
NM_000834.3:c.-19+17331_-19+17332delinsAC	NP_000825.2:n.-19+17331_-19+17332delinsAC...
XM_011520628.1:c.-19+17331_-19+17332delinsAC	XP_011518930.1:n.-19+17331_-19+17332delin...
XM_011520629.1:c.-19+17331_-19+17332delinsAC	XP_011518931.1:n.-19+17331_-19+17332delin...
XM_011520630.1:c.-19+17331_-19+17332delinsAC	XP_011518932.1:n.-19+17331_-19+17332delin...
NM_000834.4:c.-19+17331_-19+17332delinsAC	NP_000825.2:n.-19+17331_-19+17332delinsAC...
XM_011520628.2:c.-19+17331_-19+17332delinsAC	XP_011518930.1:n.-19+17331_-19+17332delin...
XM_011520629.2:c.-19+17331_-19+17332delinsAC	XP_011518931.1:n.-19+17331_-19+17332delin...
XM_017019219.2:c.-19+17331_-19+17332delinsAC	XP_016874708.1:n.-19+17331_-19+17332delin...
NM_000834.5:c.-19+17331_-19+17332delinsAC MANE Select	NP_000825.2:n.-19+17331_-19+17332delinsAC...