Canonical Allele Identifier: CA5361036

Gene: GRIN1

Linked Data

• dbSNP Id: rs773835611
• ExAC: 9:140057221 T / TGCGAGGTGA
• gnomAD v2: 9-140057221-T-TGCGAGGTGA
• gnomAD v3: 9-137162769-T-TGCGAGGTGA
• gnomAD v4: 9-137162769-T-TGCGAGGTGA
• MyVariant Identifiers: chr9:g.140057221_140057222insGCGAGGTGA (hg19) ; chr9:g.137162769_137162770insGCGAGGTGA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137162772_137162780dup , CM000671.2:g.137162772_137162780dup	GRCh38
NC_000009.11:g.140057224_140057232dup , CM000671.1:g.140057224_140057232dup	GRCh37
NC_000009.10:g.139177045_139177053dup	NCBI36
NG_011507.1:g.28616_28624dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371553.8:c.2076+33_2076+41dup	ENSP00000360608.3:n.2076+33_2076+41dup
ENST00000371560.5:c.2076+33_2076+41dup	ENSP00000360615.3:n.2076+33_2076+41dup
ENST00000371561.8:c.2013+33_2013+41dup MANE Select	ENSP00000360616.3:n.2013+33_2013+41dup
ENST00000675295.1:n.1443+33_1443+41dup
ENST00000350902.9:c.*988+33_*988+41dup	ENSP00000316915.9:n.*988+33_*988+41dup
ENST00000371546.8:c.2076+33_2076+41dup	ENSP00000360601.4:n.2076+33_2076+41dup
ENST00000371550.8:c.2013+33_2013+41dup	ENSP00000360605.4:n.2013+33_2013+41dup
ENST00000371553.7:c.2076+33_2076+41dup	ENSP00000360608.3:n.2076+33_2076+41dup
ENST00000371555.8:c.2076+33_2076+41dup	ENSP00000360610.4:n.2076+33_2076+41dup
ENST00000371559.8:c.2013+33_2013+41dup	ENSP00000360614.4:n.2013+33_2013+41dup
ENST00000371560.4:c.2076+33_2076+41dup	ENSP00000360615.3:n.2076+33_2076+41dup
ENST00000371561.7:c.2013+33_2013+41dup	ENSP00000360616.3:n.2013+33_2013+41dup
ENST00000460273.1:n.34+33_34+41dup
ENST00000471122.5:n.2090+33_2090+41dup
NM_000832.6:c.2013+33_2013+41dup	NP_000823.4:n.2013+33_2013+41dup
NM_001185090.1:c.2076+33_2076+41dup	NP_001172019.1:n.2076+33_2076+41dup
NM_001185091.1:c.2076+33_2076+41dup	NP_001172020.1:n.2076+33_2076+41dup
NM_007327.3:c.2013+33_2013+41dup	NP_015566.1:n.2013+33_2013+41dup
NM_021569.3:c.2013+33_2013+41dup	NP_067544.1:n.2013+33_2013+41dup
XM_005266071.2:c.2013+33_2013+41dup	XP_005266128.1:n.2013+33_2013+41dup
XM_005266072.2:c.2076+33_2076+41dup	XP_005266129.1:n.2076+33_2076+41dup
XM_005266073.3:c.2076+33_2076+41dup	XP_005266130.1:n.2076+33_2076+41dup
XM_011518583.1:c.2076+33_2076+41dup	XP_011516885.1:n.2076+33_2076+41dup
XM_005266071.3:c.2013+33_2013+41dup	XP_005266128.1:n.2013+33_2013+41dup
XM_005266072.3:c.2076+33_2076+41dup	XP_005266129.1:n.2076+33_2076+41dup
XM_005266073.4:c.2076+33_2076+41dup	XP_005266130.1:n.2076+33_2076+41dup
XM_011518583.2:c.2076+33_2076+41dup	XP_011516885.1:n.2076+33_2076+41dup
NM_007327.4:c.2013+33_2013+41dup MANE Select	NP_015566.1:n.2013+33_2013+41dup
NM_000832.7:c.2013+33_2013+41dup	NP_000823.4:n.2013+33_2013+41dup
NM_001185090.2:c.2076+33_2076+41dup	NP_001172019.1:n.2076+33_2076+41dup
NM_001185091.2:c.2076+33_2076+41dup	NP_001172020.1:n.2076+33_2076+41dup
NM_021569.4:c.2013+33_2013+41dup	NP_067544.1:n.2013+33_2013+41dup