Canonical Allele Identifier: CA861144607

Gene: GRIN1

Linked Data

• dbSNP Id: rs1260793707
• gnomAD v3: 9-137139294-T-TGAGCCCC
• gnomAD v4: 9-137139294-T-TGAGCCCC
• MyVariant Identifiers: chr9:g.140033746_140033747insGAGCCCC (hg19) ; chr9:g.137139294_137139295insGAGCCCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137139302_137139308dup , CM000671.2:g.137139302_137139308dup	GRCh38
NC_000009.11:g.140033754_140033760dup , CM000671.1:g.140033754_140033760dup	GRCh37
NC_000009.10:g.139153575_139153581dup	NCBI36
NG_011507.1:g.5146_5152dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371553.8:c.-185_-179dup	ENSP00000360608.3:n.-185_-179dup
ENST00000371560.5:c.-185_-179dup	ENSP00000360615.3:n.-185_-179dup
ENST00000371561.8:c.-185_-179dup MANE Select	ENSP00000360616.3:n.-185_-179dup
ENST00000350902.9:c.-185_-179dup	ENSP00000316915.9:n.-185_-179dup
ENST00000371561.7:c.-185_-179dup	ENSP00000360616.3:n.-185_-179dup
NM_000832.6:c.-185_-179dup	NP_000823.4:n.-185_-179dup
NM_001185090.1:c.-185_-179dup	NP_001172019.1:n.-185_-179dup
NM_001185091.1:c.-185_-179dup	NP_001172020.1:n.-185_-179dup
NM_007327.3:c.-185_-179dup	NP_015566.1:n.-185_-179dup
NM_021569.3:c.-185_-179dup	NP_067544.1:n.-185_-179dup
XM_005266071.2:c.-185_-179dup	XP_005266128.1:n.-185_-179dup
XM_005266072.2:c.-185_-179dup	XP_005266129.1:n.-185_-179dup
XM_005266073.3:c.-185_-179dup	XP_005266130.1:n.-185_-179dup
XM_011518583.1:c.-185_-179dup	XP_011516885.1:n.-185_-179dup
XM_005266072.3:c.-185_-179dup	XP_005266129.1:n.-185_-179dup
XM_005266073.4:c.-185_-179dup	XP_005266130.1:n.-185_-179dup
XM_011518583.2:c.-185_-179dup	XP_011516885.1:n.-185_-179dup
NM_007327.4:c.-185_-179dup MANE Select	NP_015566.1:n.-185_-179dup
NM_000832.7:c.-185_-179dup	NP_000823.4:n.-185_-179dup
NM_001185090.2:c.-185_-179dup	NP_001172019.1:n.-185_-179dup
NM_001185091.2:c.-185_-179dup	NP_001172020.1:n.-185_-179dup
NM_021569.4:c.-185_-179dup	NP_067544.1:n.-185_-179dup