Canonical Allele Identifier: CA2017525797

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13753330_13753331delinsTG , CM000674.2:g.13753330_13753331delinsTG	GRCh38
NC_000012.11:g.13906264_13906265delinsTG , CM000674.1:g.13906264_13906265delinsTG	GRCh37
NC_000012.10:g.13797531_13797532delinsTG	NCBI36
NG_031854.1:g.231758_231759delinsCA
NG_031854.2:g.233682_233683delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.996_997delinsCA MANE Select	ENSP00000477455.1:p.Ser332=
ENST00000630791.2:c.996_997delinsCA	ENSP00000486677.2:p.Ser332=
ENST00000609686.3:c.996_997delinsCA	ENSP00000477455.1:p.Ser332=
NM_000834.3:c.996_997delinsCA	NP_000825.2:p.Ser332=
XM_011520628.1:c.996_997delinsCA	XP_011518930.1:p.Ser332=
XM_011520629.1:c.996_997delinsCA	XP_011518931.1:p.Ser332=
XM_011520630.1:c.996_997delinsCA	XP_011518932.1:p.Ser332=
NM_000834.4:c.996_997delinsCA	NP_000825.2:p.Ser332=
XM_011520628.2:c.996_997delinsCA	XP_011518930.1:p.Ser332=
XM_011520629.2:c.996_997delinsCA	XP_011518931.1:p.Ser332=
XM_017019219.2:c.996_997delinsCA	XP_016874708.1:p.Ser332=
NM_000834.5:c.996_997delinsCA MANE Select	NP_000825.2:p.Ser332=