Canonical Allele Identifier: CA2617749588

Gene: GRIN2B

Linked Data

• gnomAD v4: 12-13570029-A-ACTGG

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13570029_13570030insCTGG , CM000674.2:g.13570029_13570030insCTGG	GRCh38
NC_000012.11:g.13722963_13722964insCTGG , CM000674.1:g.13722963_13722964insCTGG	GRCh37
NC_000012.10:g.13614230_13614231insCTGG	NCBI36
NG_031854.1:g.415059_415060insCCAG
NG_031854.2:g.416983_416984insCCAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000609686.4:c.2172-13_2172-12insCCAG MANE Select	ENSP00000477455.1:n.2172-13_2172-12insCCA...
ENST00000628166.2:n.432-13_432-12insCCAG
ENST00000637214.1:c.69+38573_69+38574insCCAG	ENSP00000489997.1:n.69+38573_69+38574insC...
ENST00000609686.3:c.2172-13_2172-12insCCAG	ENSP00000477455.1:n.2172-13_2172-12insCCA...
ENST00000628166.1:n.432-13_432-12insCCAG
NM_000834.3:c.2172-13_2172-12insCCAG	NP_000825.2:n.2172-13_2172-12insCCAG
XM_005253351.2:c.-43-13_-43-12insCCAG	XP_005253408.1:n.-43-13_-43-12insCCAG
XM_011520628.1:c.2172-13_2172-12insCCAG	XP_011518930.1:n.2172-13_2172-12insCCAG
XM_011520629.1:c.2172-13_2172-12insCCAG	XP_011518931.1:n.2172-13_2172-12insCCAG
XM_011520630.1:c.2172-13_2172-12insCCAG	XP_011518932.1:n.2172-13_2172-12insCCAG
NM_000834.4:c.2172-13_2172-12insCCAG	NP_000825.2:n.2172-13_2172-12insCCAG
XM_005253351.3:c.-43-13_-43-12insCCAG	XP_005253408.1:n.-43-13_-43-12insCCAG
XM_011520628.2:c.2172-13_2172-12insCCAG	XP_011518930.1:n.2172-13_2172-12insCCAG
XM_011520629.2:c.2172-13_2172-12insCCAG	XP_011518931.1:n.2172-13_2172-12insCCAG
XM_017019219.2:c.2172-13_2172-12insCCAG	XP_016874708.1:n.2172-13_2172-12insCCAG
NM_000834.5:c.2172-13_2172-12insCCAG MANE Select	NP_000825.2:n.2172-13_2172-12insCCAG