Canonical Allele Identifier: CA2695216124

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13611750del , CM000674.2:g.13611750del	GRCh38
NC_000012.11:g.13764684del , CM000674.1:g.13764684del	GRCh37
NC_000012.10:g.13655951del	NCBI36
NG_031854.1:g.373339del
NG_031854.2:g.375263del

Transcript Alleles

HGVS	Amino-acid change
ENST00000609686.4:c.1755del MANE Select	ENSP00000477455.1:p.Tyr585Ter
ENST00000609686.3:c.1755del	ENSP00000477455.1:p.Tyr585Ter
NM_000834.3:c.1755del	NP_000825.2:p.Tyr585Ter
XM_011520628.1:c.1755del	XP_011518930.1:p.Tyr585Ter
XM_011520629.1:c.1755del	XP_011518931.1:p.Tyr585Ter
XM_011520630.1:c.1755del	XP_011518932.1:p.Tyr585Ter
XR_931372.1:n.179-3348del
XR_931373.1:n.318+2993del
XR_931374.1:n.117+1150del
NM_000834.4:c.1755del	NP_000825.2:p.Tyr585Ter
XM_011520628.2:c.1755del	XP_011518930.1:p.Tyr585Ter
XM_011520629.2:c.1755del	XP_011518931.1:p.Tyr585Ter
XM_017019219.2:c.1755del	XP_016874708.1:p.Tyr585Ter
XR_001749013.1:n.599+1150del
XR_931372.2:n.316-3348del
XR_931373.2:n.457+2993del
NM_000834.5:c.1755del MANE Select	NP_000825.2:p.Tyr585Ter