Canonical Allele Identifier: CA591372788

Gene: GRIN1

Linked Data

• dbSNP Id: rs1339163613
• gnomAD v2: 9-140052712-A-AGAAGGAGCAGGGAGAAGGAGCAGGGG
• gnomAD v3: 9-137158260-A-AGAAGGAGCAGGGAGAAGGAGCAGGGG
• gnomAD v4: 9-137158260-A-AGAAGGAGCAGGGAGAAGGAGCAGGGG
• MyVariant Identifiers: chr9:g.140052738_140052739insGAAGGAGCAGGGAGAAGGAGCAGGGG (hg19) ; chr9:g.137158286_137158287insGAAGGAGCAGGGAGAAGGAGCAGGGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137158278_137158303dup , CM000671.2:g.137158278_137158303dup	GRCh38
NC_000009.11:g.140052730_140052755dup , CM000671.1:g.140052730_140052755dup	GRCh37
NC_000009.10:g.139172551_139172576dup	NCBI36
NG_011507.1:g.24122_24147dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371553.8:c.1032-101_1032-76dup	ENSP00000360608.3:n.1032-101_1032-76dup
ENST00000371560.5:c.1032-101_1032-76dup	ENSP00000360615.3:n.1032-101_1032-76dup
ENST00000371561.8:c.969-101_969-76dup MANE Select	ENSP00000360616.3:n.969-101_969-76dup
ENST00000675295.1:n.399-101_399-76dup
ENST00000676396.1:n.2479-101_2479-76dup
ENST00000350902.9:c.1015-101_1015-76dup	ENSP00000316915.9:n.1015-101_1015-76dup
ENST00000371546.8:c.1032-101_1032-76dup	ENSP00000360601.4:n.1032-101_1032-76dup
ENST00000371550.8:c.969-101_969-76dup	ENSP00000360605.4:n.969-101_969-76dup
ENST00000371553.7:c.1032-101_1032-76dup	ENSP00000360608.3:n.1032-101_1032-76dup
ENST00000371555.8:c.1032-101_1032-76dup	ENSP00000360610.4:n.1032-101_1032-76dup
ENST00000371559.8:c.969-101_969-76dup	ENSP00000360614.4:n.969-101_969-76dup
ENST00000371560.4:c.1032-101_1032-76dup	ENSP00000360615.3:n.1032-101_1032-76dup
ENST00000371561.7:c.969-101_969-76dup	ENSP00000360616.3:n.969-101_969-76dup
ENST00000471122.5:n.1046-101_1046-76dup
ENST00000485413.1:n.63-101_63-76dup
NM_000832.6:c.969-101_969-76dup	NP_000823.4:n.969-101_969-76dup
NM_001185090.1:c.1032-101_1032-76dup	NP_001172019.1:n.1032-101_1032-76dup
NM_001185091.1:c.1032-101_1032-76dup	NP_001172020.1:n.1032-101_1032-76dup
NM_007327.3:c.969-101_969-76dup	NP_015566.1:n.969-101_969-76dup
NM_021569.3:c.969-101_969-76dup	NP_067544.1:n.969-101_969-76dup
XM_005266071.2:c.969-101_969-76dup	XP_005266128.1:n.969-101_969-76dup
XM_005266072.2:c.1032-101_1032-76dup	XP_005266129.1:n.1032-101_1032-76dup
XM_005266073.3:c.1032-101_1032-76dup	XP_005266130.1:n.1032-101_1032-76dup
XM_011518583.1:c.1032-101_1032-76dup	XP_011516885.1:n.1032-101_1032-76dup
XM_005266071.3:c.969-101_969-76dup	XP_005266128.1:n.969-101_969-76dup
XM_005266072.3:c.1032-101_1032-76dup	XP_005266129.1:n.1032-101_1032-76dup
XM_005266073.4:c.1032-101_1032-76dup	XP_005266130.1:n.1032-101_1032-76dup
XM_011518583.2:c.1032-101_1032-76dup	XP_011516885.1:n.1032-101_1032-76dup
NM_007327.4:c.969-101_969-76dup MANE Select	NP_015566.1:n.969-101_969-76dup
NM_000832.7:c.969-101_969-76dup	NP_000823.4:n.969-101_969-76dup
NM_001185090.2:c.1032-101_1032-76dup	NP_001172019.1:n.1032-101_1032-76dup
NM_001185091.2:c.1032-101_1032-76dup	NP_001172020.1:n.1032-101_1032-76dup
NM_021569.4:c.969-101_969-76dup	NP_067544.1:n.969-101_969-76dup