Canonical Allele Identifier: CA591372594

Gene: GRIN1

Linked Data

• ClinVar Variation Id: 2112023
• ClinVar RCV Id: RCV003024123
• dbSNP Id: rs1564357925
• gnomAD v2: 9-140051490-G-GTGGGCGGGGCCTCCCCGGAGC
• gnomAD v4: 9-137157038-G-GTGGGCGGGGCCTCCCCGGAGC
• MyVariant Identifiers: chr9:g.140051511_140051512insTGGGCGGGGCCTCCCCGGAGC (hg19) ; chr9:g.137157059_137157060insTGGGCGGGGCCTCCCCGGAGC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137157049_137157069dup , CM000671.2:g.137157049_137157069dup	GRCh38
NC_000009.11:g.140051501_140051521dup , CM000671.1:g.140051501_140051521dup	GRCh37
NC_000009.10:g.139171322_139171342dup	NCBI36
NG_011507.1:g.22893_22913dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371553.8:c.1031+12_1031+32dup	ENSP00000360608.3:n.1031+12_1031+32dup
ENST00000371560.5:c.1031+12_1031+32dup	ENSP00000360615.3:n.1031+12_1031+32dup
ENST00000371561.8:c.968+12_968+32dup MANE Select	ENSP00000360616.3:n.968+12_968+32dup
ENST00000675295.1:n.398+12_398+32dup
ENST00000676396.1:n.2478+12_2478+32dup
ENST00000350902.9:c.1014+12_1014+32dup	ENSP00000316915.9:n.1014+12_1014+32dup
ENST00000371546.8:c.1031+12_1031+32dup	ENSP00000360601.4:n.1031+12_1031+32dup
ENST00000371550.8:c.968+12_968+32dup	ENSP00000360605.4:n.968+12_968+32dup
ENST00000371553.7:c.1031+12_1031+32dup	ENSP00000360608.3:n.1031+12_1031+32dup
ENST00000371555.8:c.1031+12_1031+32dup	ENSP00000360610.4:n.1031+12_1031+32dup
ENST00000371559.8:c.968+12_968+32dup	ENSP00000360614.4:n.968+12_968+32dup
ENST00000371560.4:c.1031+12_1031+32dup	ENSP00000360615.3:n.1031+12_1031+32dup
ENST00000371561.7:c.968+12_968+32dup	ENSP00000360616.3:n.968+12_968+32dup
ENST00000471122.5:n.1045+12_1045+32dup
ENST00000485413.1:n.62+12_62+32dup
NM_000832.6:c.968+12_968+32dup	NP_000823.4:n.968+12_968+32dup
NM_001185090.1:c.1031+12_1031+32dup	NP_001172019.1:n.1031+12_1031+32dup
NM_001185091.1:c.1031+12_1031+32dup	NP_001172020.1:n.1031+12_1031+32dup
NM_007327.3:c.968+12_968+32dup	NP_015566.1:n.968+12_968+32dup
NM_021569.3:c.968+12_968+32dup	NP_067544.1:n.968+12_968+32dup
XM_005266071.2:c.968+12_968+32dup	XP_005266128.1:n.968+12_968+32dup
XM_005266072.2:c.1031+12_1031+32dup	XP_005266129.1:n.1031+12_1031+32dup
XM_005266073.3:c.1031+12_1031+32dup	XP_005266130.1:n.1031+12_1031+32dup
XM_011518583.1:c.1031+12_1031+32dup	XP_011516885.1:n.1031+12_1031+32dup
XM_005266071.3:c.968+12_968+32dup	XP_005266128.1:n.968+12_968+32dup
XM_005266072.3:c.1031+12_1031+32dup	XP_005266129.1:n.1031+12_1031+32dup
XM_005266073.4:c.1031+12_1031+32dup	XP_005266130.1:n.1031+12_1031+32dup
XM_011518583.2:c.1031+12_1031+32dup	XP_011516885.1:n.1031+12_1031+32dup
NM_007327.4:c.968+12_968+32dup MANE Select	NP_015566.1:n.968+12_968+32dup
NM_000832.7:c.968+12_968+32dup	NP_000823.4:n.968+12_968+32dup
NM_001185090.2:c.1031+12_1031+32dup	NP_001172019.1:n.1031+12_1031+32dup
NM_001185091.2:c.1031+12_1031+32dup	NP_001172020.1:n.1031+12_1031+32dup
NM_021569.4:c.968+12_968+32dup	NP_067544.1:n.968+12_968+32dup