Canonical Allele Identifier: CA2017447978

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13608842_13608844delinsCAA , CM000674.2:g.13608842_13608844delinsCAA	GRCh38
NC_000012.11:g.13761776_13761778delinsCAA , CM000674.1:g.13761776_13761778delinsCAA	GRCh37
NC_000012.10:g.13653043_13653045delinsCAA	NCBI36
NG_031854.1:g.376245_376247delinsTTG
NG_031854.2:g.378169_378171delinsTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1781-12_1781-10delinsTTG MANE Select	ENSP00000477455.1:n.1781-12_1781-10delinsTTG
ENST00000628166.2:n.41-12_41-10delinsTTG
ENST00000609686.3:c.1781-12_1781-10delinsTTG	ENSP00000477455.1:n.1781-12_1781-10delinsTTG
ENST00000628166.1:n.41-12_41-10delinsTTG
NM_000834.3:c.1781-12_1781-10delinsTTG	NP_000825.2:n.1781-12_1781-10delinsTTG
XM_011520628.1:c.1781-12_1781-10delinsTTG	XP_011518930.1:n.1781-12_1781-10delinsTTG
XM_011520629.1:c.1781-12_1781-10delinsTTG	XP_011518931.1:n.1781-12_1781-10delinsTTG
XM_011520630.1:c.1781-12_1781-10delinsTTG	XP_011518932.1:n.1781-12_1781-10delinsTTG
XR_931372.1:n.179-6256_179-6254delinsCAA
XR_931373.1:n.318+85_318+87delinsCAA
NM_000834.4:c.1781-12_1781-10delinsTTG	NP_000825.2:n.1781-12_1781-10delinsTTG
XM_011520628.2:c.1781-12_1781-10delinsTTG	XP_011518930.1:n.1781-12_1781-10delinsTTG
XM_011520629.2:c.1781-12_1781-10delinsTTG	XP_011518931.1:n.1781-12_1781-10delinsTTG
XM_017019219.2:c.1781-12_1781-10delinsTTG	XP_016874708.1:n.1781-12_1781-10delinsTTG
XR_001749013.1:n.457+85_457+87delinsCAA
XR_931372.2:n.316-6256_316-6254delinsCAA
XR_931373.2:n.457+85_457+87delinsCAA
NM_000834.5:c.1781-12_1781-10delinsTTG MANE Select	NP_000825.2:n.1781-12_1781-10delinsTTG