Canonical Allele Identifier: CA2017440503

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13570033_13570037delinsGCAAA , CM000674.2:g.13570033_13570037delinsGCAAA	GRCh38
NC_000012.11:g.13722967_13722971delinsGCAAA , CM000674.1:g.13722967_13722971delinsGCAAA	GRCh37
NC_000012.10:g.13614234_13614238delinsGCAAA	NCBI36
NG_031854.1:g.415052_415056delinsTTTGC
NG_031854.2:g.416976_416980delinsTTTGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000609686.4:c.2172-20_2172-16delinsTTTGC MANE Select	ENSP00000477455.1:n.2172-20_2172-16delins...
ENST00000628166.2:n.432-20_432-16delinsTTTGC
ENST00000637214.1:c.69+38566_69+38570delinsTTTGC	ENSP00000489997.1:n.69+38566_69+38570deli...
ENST00000609686.3:c.2172-20_2172-16delinsTTTGC	ENSP00000477455.1:n.2172-20_2172-16delins...
ENST00000628166.1:n.432-20_432-16delinsTTTGC
NM_000834.3:c.2172-20_2172-16delinsTTTGC	NP_000825.2:n.2172-20_2172-16delinsTTTGC
XM_005253351.2:c.-43-20_-43-16delinsTTTGC	XP_005253408.1:n.-43-20_-43-16delinsTTTGC...
XM_011520628.1:c.2172-20_2172-16delinsTTTGC	XP_011518930.1:n.2172-20_2172-16delinsTTT...
XM_011520629.1:c.2172-20_2172-16delinsTTTGC	XP_011518931.1:n.2172-20_2172-16delinsTTT...
XM_011520630.1:c.2172-20_2172-16delinsTTTGC	XP_011518932.1:n.2172-20_2172-16delinsTTT...
NM_000834.4:c.2172-20_2172-16delinsTTTGC	NP_000825.2:n.2172-20_2172-16delinsTTTGC
XM_005253351.3:c.-43-20_-43-16delinsTTTGC	XP_005253408.1:n.-43-20_-43-16delinsTTTGC...
XM_011520628.2:c.2172-20_2172-16delinsTTTGC	XP_011518930.1:n.2172-20_2172-16delinsTTT...
XM_011520629.2:c.2172-20_2172-16delinsTTTGC	XP_011518931.1:n.2172-20_2172-16delinsTTT...
XM_017019219.2:c.2172-20_2172-16delinsTTTGC	XP_016874708.1:n.2172-20_2172-16delinsTTT...
NM_000834.5:c.2172-20_2172-16delinsTTTGC MANE Select	NP_000825.2:n.2172-20_2172-16delinsTTTGC