Canonical Allele Identifier: CA2558122254

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13608747_13608748insA , CM000674.2:g.13608747_13608748insA	GRCh38
NC_000012.11:g.13761681_13761682insA , CM000674.1:g.13761681_13761682insA	GRCh37
NC_000012.10:g.13652948_13652949insA	NCBI36
NG_031854.1:g.376341_376342insT
NG_031854.2:g.378265_378266insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1865_1866insT MANE Select	ENSP00000477455.1:p.Thr626AspfsTer?
ENST00000628166.2:n.125_126insT
ENST00000609686.3:c.1865_1866insT	ENSP00000477455.1:p.Thr626AspfsTer?
ENST00000628166.1:n.125_126insT
NM_000834.3:c.1865_1866insT	NP_000825.2:p.Thr626AspfsTer?
XM_011520628.1:c.1865_1866insT	XP_011518930.1:p.Thr626AspfsTer?
XM_011520629.1:c.1865_1866insT	XP_011518931.1:p.Thr626AspfsTer?
XM_011520630.1:c.1865_1866insT	XP_011518932.1:p.Thr626AspfsTer?
XR_931372.1:n.179-6351_179-6350insA
XR_931373.1:n.308_309insA
NM_000834.4:c.1865_1866insT	NP_000825.2:p.Thr626AspfsTer?
XM_011520628.2:c.1865_1866insT	XP_011518930.1:p.Thr626AspfsTer?
XM_011520629.2:c.1865_1866insT	XP_011518931.1:p.Thr626AspfsTer?
XM_017019219.2:c.1865_1866insT	XP_016874708.1:p.Thr626AspfsTer?
XR_001749013.1:n.447_448insA
XR_931372.2:n.316-6351_316-6350insA
XR_931373.2:n.447_448insA
NM_000834.5:c.1865_1866insT MANE Select	NP_000825.2:p.Thr626AspfsTer?