Canonical Allele Identifier: CA2695216105

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13608786_13608794del , CM000674.2:g.13608786_13608794del	GRCh38
NC_000012.11:g.13761720_13761728del , CM000674.1:g.13761720_13761728del	GRCh37
NC_000012.10:g.13652987_13652995del	NCBI36
NG_031854.1:g.376298_376306del
NG_031854.2:g.378222_378230del

Transcript Alleles

HGVS	Amino-acid change
ENST00000609686.4:c.1822_1830del MANE Select	ENSP00000477455.1:p.Leu608_Trp610del
ENST00000628166.2:n.82_90del
ENST00000609686.3:c.1822_1830del	ENSP00000477455.1:p.Leu608_Trp610del
ENST00000628166.1:n.82_90del
NM_000834.3:c.1822_1830del	NP_000825.2:p.Leu608_Trp610del
XM_011520628.1:c.1822_1830del	XP_011518930.1:p.Leu608_Trp610del
XM_011520629.1:c.1822_1830del	XP_011518931.1:p.Leu608_Trp610del
XM_011520630.1:c.1822_1830del	XP_011518932.1:p.Leu608_Trp610del
XR_931372.1:n.179-6312_179-6304del
XR_931373.1:n.318+29_318+37del
NM_000834.4:c.1822_1830del	NP_000825.2:p.Leu608_Trp610del
XM_011520628.2:c.1822_1830del	XP_011518930.1:p.Leu608_Trp610del
XM_011520629.2:c.1822_1830del	XP_011518931.1:p.Leu608_Trp610del
XM_017019219.2:c.1822_1830del	XP_016874708.1:p.Leu608_Trp610del
XR_001749013.1:n.457+29_457+37del
XR_931372.2:n.316-6312_316-6304del
XR_931373.2:n.457+29_457+37del
NM_000834.5:c.1822_1830del MANE Select	NP_000825.2:p.Leu608_Trp610del