Canonical Allele Identifier: CA2017417789

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13564147_13564150delinsTGGA , CM000674.2:g.13564147_13564150delinsTGGA	GRCh38
NC_000012.11:g.13717081_13717084delinsTGGA , CM000674.1:g.13717081_13717084delinsTGGA	GRCh37
NC_000012.10:g.13608348_13608351delinsTGGA	NCBI36
NG_031854.1:g.420939_420942delinsTCCA
NG_031854.2:g.422863_422866delinsTCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.3088_3091delinsTCCA MANE Select	ENSP00000477455.1:p.Ser1030=
ENST00000637214.1:c.69+44453_69+44456delinsTCCA	ENSP00000489997.1:n.69+44453_69+44456delinsTCCA
ENST00000609686.3:c.3088_3091delinsTCCA	ENSP00000477455.1:p.Ser1030=
ENST00000628166.1:n.1348_1351delinsTCCA
NM_000834.3:c.3088_3091delinsTCCA	NP_000825.2:p.Ser1030=
XM_005253351.2:c.874_877delinsTCCA	XP_005253408.1:p.Ser292=
XM_011520628.1:c.3088_3091delinsTCCA	XP_011518930.1:p.Ser1030=
XM_011520629.1:c.3088_3091delinsTCCA	XP_011518931.1:p.Ser1030=
XM_011520630.1:c.3088_3091delinsTCCA	XP_011518932.1:p.Ser1030=
NM_000834.4:c.3088_3091delinsTCCA	NP_000825.2:p.Ser1030=
XM_005253351.3:c.874_877delinsTCCA	XP_005253408.1:p.Ser292=
XM_011520628.2:c.3088_3091delinsTCCA	XP_011518930.1:p.Ser1030=
XM_011520629.2:c.3088_3091delinsTCCA	XP_011518931.1:p.Ser1030=
XM_017019219.2:c.3088_3091delinsTCCA	XP_016874708.1:p.Ser1030=
NM_000834.5:c.3088_3091delinsTCCA MANE Select	NP_000825.2:p.Ser1030=