Canonical Allele Identifier: CA2017622207

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13962586_13962587delinsCA , CM000674.2:g.13962586_13962587delinsCA	GRCh38
NC_000012.11:g.14115520_14115521delinsCA , CM000674.1:g.14115520_14115521delinsCA	GRCh37
NC_000012.10:g.14006787_14006788delinsCA	NCBI36
NG_031854.1:g.22502_22503delinsTG
NG_031854.2:g.24426_24427delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000609686.4:c.-19+17341_-19+17342delinsTG MANE Select	ENSP00000477455.1:n.-19+17341_-19+17342de...
ENST00000630791.2:c.-19+17341_-19+17342delinsTG	ENSP00000486677.2:n.-19+17341_-19+17342de...
ENST00000609686.3:c.-19+17341_-19+17342delinsTG	ENSP00000477455.1:n.-19+17341_-19+17342de...
ENST00000627535.2:c.-19+17341_-19+17342delinsTG	ENSP00000486411.1:n.-19+17341_-19+17342de...
ENST00000630791.1:c.-19+17341_-19+17342delinsTG	ENSP00000486677.1:n.-19+17341_-19+17342de...
NM_000834.3:c.-19+17341_-19+17342delinsTG	NP_000825.2:n.-19+17341_-19+17342delinsTG...
XM_011520628.1:c.-19+17341_-19+17342delinsTG	XP_011518930.1:n.-19+17341_-19+17342delin...
XM_011520629.1:c.-19+17341_-19+17342delinsTG	XP_011518931.1:n.-19+17341_-19+17342delin...
XM_011520630.1:c.-19+17341_-19+17342delinsTG	XP_011518932.1:n.-19+17341_-19+17342delin...
NM_000834.4:c.-19+17341_-19+17342delinsTG	NP_000825.2:n.-19+17341_-19+17342delinsTG...
XM_011520628.2:c.-19+17341_-19+17342delinsTG	XP_011518930.1:n.-19+17341_-19+17342delin...
XM_011520629.2:c.-19+17341_-19+17342delinsTG	XP_011518931.1:n.-19+17341_-19+17342delin...
XM_017019219.2:c.-19+17341_-19+17342delinsTG	XP_016874708.1:n.-19+17341_-19+17342delin...
NM_000834.5:c.-19+17341_-19+17342delinsTG MANE Select	NP_000825.2:n.-19+17341_-19+17342delinsTG...