Canonical Allele Identifier: CA2741232247

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13944699_13944702del , CM000674.2:g.13944699_13944702del	GRCh38
NC_000012.11:g.14097633_14097636del , CM000674.1:g.14097633_14097636del	GRCh37
NC_000012.10:g.13988900_13988903del	NCBI36
NG_031854.1:g.40393_40396del
NG_031854.2:g.42317_42320del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.-19+35232_-19+35235del MANE Select	ENSP00000477455.1:n.-19+35232_-19+35235del
ENST00000630791.2:c.-19+35232_-19+35235del	ENSP00000486677.2:n.-19+35232_-19+35235del
ENST00000609686.3:c.-19+35232_-19+35235del	ENSP00000477455.1:n.-19+35232_-19+35235del
ENST00000627535.2:c.-19+35232_-19+35235del	ENSP00000486411.1:n.-19+35232_-19+35235del
ENST00000630791.1:c.-19+35232_-19+35235del	ENSP00000486677.1:n.-19+35232_-19+35235del
NM_000834.3:c.-19+35232_-19+35235del	NP_000825.2:n.-19+35232_-19+35235del
XM_011520628.1:c.-19+35232_-19+35235del	XP_011518930.1:n.-19+35232_-19+35235del
XM_011520629.1:c.-19+35232_-19+35235del	XP_011518931.1:n.-19+35232_-19+35235del
XM_011520630.1:c.-19+35232_-19+35235del	XP_011518932.1:n.-19+35232_-19+35235del
NM_000834.4:c.-19+35232_-19+35235del	NP_000825.2:n.-19+35232_-19+35235del
XM_011520628.2:c.-19+35232_-19+35235del	XP_011518930.1:n.-19+35232_-19+35235del
XM_011520629.2:c.-19+35232_-19+35235del	XP_011518931.1:n.-19+35232_-19+35235del
XM_017019219.2:c.-19+35232_-19+35235del	XP_016874708.1:n.-19+35232_-19+35235del
NM_000834.5:c.-19+35232_-19+35235del MANE Select	NP_000825.2:n.-19+35232_-19+35235del