Canonical Allele Identifier: CA2695216101

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13569834del , CM000674.2:g.13569834del	GRCh38
NC_000012.11:g.13722768del , CM000674.1:g.13722768del	GRCh37
NC_000012.10:g.13614035del	NCBI36
NG_031854.1:g.415255del
NG_031854.2:g.417179del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.2355del MANE Select	ENSP00000477455.1:p.Asp786MetfsTer24
ENST00000628166.2:n.615del
ENST00000637214.1:c.69+38769del	ENSP00000489997.1:n.69+38769del
ENST00000609686.3:c.2355del	ENSP00000477455.1:p.Asp786MetfsTer24
ENST00000628166.1:n.615del
NM_000834.3:c.2355del	NP_000825.2:p.Asp786MetfsTer24
XM_005253351.2:c.141del	XP_005253408.1:p.Asp48MetfsTer24
XM_011520628.1:c.2355del	XP_011518930.1:p.Asp786MetfsTer24
XM_011520629.1:c.2355del	XP_011518931.1:p.Asp786MetfsTer24
XM_011520630.1:c.2355del	XP_011518932.1:p.Asp786MetfsTer24
NM_000834.4:c.2355del	NP_000825.2:p.Asp786MetfsTer24
XM_005253351.3:c.141del	XP_005253408.1:p.Asp48MetfsTer24
XM_011520628.2:c.2355del	XP_011518930.1:p.Asp786MetfsTer24
XM_011520629.2:c.2355del	XP_011518931.1:p.Asp786MetfsTer24
XM_017019219.2:c.2355del	XP_016874708.1:p.Asp786MetfsTer24
NM_000834.5:c.2355del MANE Select	NP_000825.2:p.Asp786MetfsTer24