Canonical Allele Identifier: CA2017463514

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13615696_13615700delinsCAAAA , CM000674.2:g.13615696_13615700delinsCAAAA	GRCh38
NC_000012.11:g.13768630_13768634delinsCAAAA , CM000674.1:g.13768630_13768634delinsCAAAA	GRCh37
NC_000012.10:g.13659897_13659901delinsCAAAA	NCBI36
NG_031854.1:g.369389_369393delinsTTTTG
NG_031854.2:g.371313_371317delinsTTTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1329-36_1329-32delinsTTTTG MANE Select	ENSP00000477455.1:n.1329-36_1329-32delinsTTTTG
ENST00000630791.2:c.1329-36_1329-32delinsTTTTG	ENSP00000486677.2:n.1329-36_1329-32delinsTTTTG
ENST00000609686.3:c.1329-36_1329-32delinsTTTTG	ENSP00000477455.1:n.1329-36_1329-32delinsTTTTG
NM_000834.3:c.1329-36_1329-32delinsTTTTG	NP_000825.2:n.1329-36_1329-32delinsTTTTG
XM_011520628.1:c.1329-36_1329-32delinsTTTTG	XP_011518930.1:n.1329-36_1329-32delinsTTTTG
XM_011520629.1:c.1329-36_1329-32delinsTTTTG	XP_011518931.1:n.1329-36_1329-32delinsTTTTG
XM_011520630.1:c.1329-36_1329-32delinsTTTTG	XP_011518932.1:n.1329-36_1329-32delinsTTTTG
XR_931372.1:n.307+470_307+474delinsCAAAA
XR_931373.1:n.447+470_447+474delinsCAAAA
XR_931374.1:n.246+470_246+474delinsCAAAA
NM_000834.4:c.1329-36_1329-32delinsTTTTG	NP_000825.2:n.1329-36_1329-32delinsTTTTG
XM_011520628.2:c.1329-36_1329-32delinsTTTTG	XP_011518930.1:n.1329-36_1329-32delinsTTTTG
XM_011520629.2:c.1329-36_1329-32delinsTTTTG	XP_011518931.1:n.1329-36_1329-32delinsTTTTG
XM_017019219.2:c.1329-36_1329-32delinsTTTTG	XP_016874708.1:n.1329-36_1329-32delinsTTTTG
XR_001749013.1:n.728+470_728+474delinsCAAAA
XR_931372.2:n.444+470_444+474delinsCAAAA
XR_931373.2:n.586+470_586+474delinsCAAAA
NM_000834.5:c.1329-36_1329-32delinsTTTTG MANE Select	NP_000825.2:n.1329-36_1329-32delinsTTTTG