Canonical Allele Identifier: CA2017525816

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13753382_13753383delinsAG , CM000674.2:g.13753382_13753383delinsAG	GRCh38
NC_000012.11:g.13906316_13906317delinsAG , CM000674.1:g.13906316_13906317delinsAG	GRCh37
NC_000012.10:g.13797583_13797584delinsAG	NCBI36
NG_031854.1:g.231706_231707delinsCT
NG_031854.2:g.233630_233631delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.944_945delinsCT MANE Select	ENSP00000477455.1:p.Pro315=
ENST00000630791.2:c.944_945delinsCT	ENSP00000486677.2:p.Pro315=
ENST00000609686.3:c.944_945delinsCT	ENSP00000477455.1:p.Pro315=
NM_000834.3:c.944_945delinsCT	NP_000825.2:p.Pro315=
XM_011520628.1:c.944_945delinsCT	XP_011518930.1:p.Pro315=
XM_011520629.1:c.944_945delinsCT	XP_011518931.1:p.Pro315=
XM_011520630.1:c.944_945delinsCT	XP_011518932.1:p.Pro315=
NM_000834.4:c.944_945delinsCT	NP_000825.2:p.Pro315=
XM_011520628.2:c.944_945delinsCT	XP_011518930.1:p.Pro315=
XM_011520629.2:c.944_945delinsCT	XP_011518931.1:p.Pro315=
XM_017019219.2:c.944_945delinsCT	XP_016874708.1:p.Pro315=
NM_000834.5:c.944_945delinsCT MANE Select	NP_000825.2:p.Pro315=