Canonical Allele Identifier: CA2017448138

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13608987_13608989delinsATC , CM000674.2:g.13608987_13608989delinsATC	GRCh38
NC_000012.11:g.13761921_13761923delinsATC , CM000674.1:g.13761921_13761923delinsATC	GRCh37
NC_000012.10:g.13653188_13653190delinsATC	NCBI36
NG_031854.1:g.376100_376102delinsGAT
NG_031854.2:g.378024_378026delinsGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1781-157_1781-155delinsGAT MANE Select	ENSP00000477455.1:n.1781-157_1781-155delinsGAT
ENST00000628166.2:n.41-157_41-155delinsGAT
ENST00000609686.3:c.1781-157_1781-155delinsGAT	ENSP00000477455.1:n.1781-157_1781-155delinsGAT
ENST00000628166.1:n.41-157_41-155delinsGAT
NM_000834.3:c.1781-157_1781-155delinsGAT	NP_000825.2:n.1781-157_1781-155delinsGAT
XM_011520628.1:c.1781-157_1781-155delinsGAT	XP_011518930.1:n.1781-157_1781-155delinsGAT
XM_011520629.1:c.1781-157_1781-155delinsGAT	XP_011518931.1:n.1781-157_1781-155delinsGAT
XM_011520630.1:c.1781-157_1781-155delinsGAT	XP_011518932.1:n.1781-157_1781-155delinsGAT
XR_931372.1:n.179-6111_179-6109delinsATC
XR_931373.1:n.318+230_318+232delinsATC
NM_000834.4:c.1781-157_1781-155delinsGAT	NP_000825.2:n.1781-157_1781-155delinsGAT
XM_011520628.2:c.1781-157_1781-155delinsGAT	XP_011518930.1:n.1781-157_1781-155delinsGAT
XM_011520629.2:c.1781-157_1781-155delinsGAT	XP_011518931.1:n.1781-157_1781-155delinsGAT
XM_017019219.2:c.1781-157_1781-155delinsGAT	XP_016874708.1:n.1781-157_1781-155delinsGAT
XR_001749013.1:n.457+230_457+232delinsATC
XR_931372.2:n.316-6111_316-6109delinsATC
XR_931373.2:n.457+230_457+232delinsATC
NM_000834.5:c.1781-157_1781-155delinsGAT MANE Select	NP_000825.2:n.1781-157_1781-155delinsGAT