Canonical Allele Identifier: CA1884328214
Gene: GRIN1 HGNC NCBI

Linked Data

dbSNP Id: rs1833273067

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137157132_137157133insTGGGGTCACTCCAGAGATGGGCGGGGCCGCTCTTGGGGAGGTGGG , CM000671.2:g.137157132_137157133insTGGGGTCACTCCAGAGATGGGCGGGGCCGCTCTTGGGGAGGTGGG GRCh38
NC_000009.11:g.140051584_140051585insTGGGGTCACTCCAGAGATGGGCGGGGCCGCTCTTGGGGAGGTGGG , CM000671.1:g.140051584_140051585insTGGGGTCACTCCAGAGATGGGCGGGGCCGCTCTTGGGGAGGTGGG GRCh37
NC_000009.10:g.139171405_139171406insTGGGGTCACTCCAGAGATGGGCGGGGCCGCTCTTGGGGAGGTGGG NCBI36
NG_011507.1:g.22976_22977insTGGGGTCACTCCAGAGATGGGCGGGGCCGCTCTTGGGGAGGTGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000371553.8:c.1031+95_1031+96insTGGGGTCACTCCAGAGATGGGCGGGGCCGCTCTTGGGGAGGTGGG ENSP00000360608.3:n.1031+95_1031+96insTGGGGTCACTCCAGAGATGGGCG...
ENST00000371560.5:c.1031+95_1031+96insTGGGGTCACTCCAGAGATGGGCGGGGCCGCTCTTGGGGAGGTGGG ENSP00000360615.3:n.1031+95_1031+96insTGGGGTCACTCCAGAGATGGGCG...
ENST00000371561.8:c.968+95_968+96insTGGGGTCACTCCAGAGATGGGCGGGGCCGCTCTTGGGGAGGTGGG MANE Select ENSP00000360616.3:n.968+95_968+96insTGGGGTCACTCCAGAGATGGGCGGG...
ENST00000675295.1:n.398+95_398+96insTGGGGTCACTCCAGAGATGGGCGGGGCCGCTCTTGGGGAGGTGGG
ENST00000676396.1:n.2478+95_2478+96insTGGGGTCACTCCAGAGATGGGCGGGGCCGCTCTTGGGGAGGTGGG
ENST00000350902.9:c.1014+95_1014+96insTGGGGTCACTCCAGAGATGGGCGGGGCCGCTCTTGGGGAGGTGGG ENSP00000316915.9:n.1014+95_1014+96insTGGGGTCACTCCAGAGATGGGCG...
ENST00000371546.8:c.1031+95_1031+96insTGGGGTCACTCCAGAGATGGGCGGGGCCGCTCTTGGGGAGGTGGG ENSP00000360601.4:n.1031+95_1031+96insTGGGGTCACTCCAGAGATGGGCG...
ENST00000371550.8:c.968+95_968+96insTGGGGTCACTCCAGAGATGGGCGGGGCCGCTCTTGGGGAGGTGGG ENSP00000360605.4:n.968+95_968+96insTGGGGTCACTCCAGAGATGGGCGGG...
ENST00000371553.7:c.1031+95_1031+96insTGGGGTCACTCCAGAGATGGGCGGGGCCGCTCTTGGGGAGGTGGG ENSP00000360608.3:n.1031+95_1031+96insTGGGGTCACTCCAGAGATGGGCG...
ENST00000371555.8:c.1031+95_1031+96insTGGGGTCACTCCAGAGATGGGCGGGGCCGCTCTTGGGGAGGTGGG ENSP00000360610.4:n.1031+95_1031+96insTGGGGTCACTCCAGAGATGGGCG...
ENST00000371559.8:c.968+95_968+96insTGGGGTCACTCCAGAGATGGGCGGGGCCGCTCTTGGGGAGGTGGG ENSP00000360614.4:n.968+95_968+96insTGGGGTCACTCCAGAGATGGGCGGG...
ENST00000371560.4:c.1031+95_1031+96insTGGGGTCACTCCAGAGATGGGCGGGGCCGCTCTTGGGGAGGTGGG ENSP00000360615.3:n.1031+95_1031+96insTGGGGTCACTCCAGAGATGGGCG...
ENST00000371561.7:c.968+95_968+96insTGGGGTCACTCCAGAGATGGGCGGGGCCGCTCTTGGGGAGGTGGG ENSP00000360616.3:n.968+95_968+96insTGGGGTCACTCCAGAGATGGGCGGG...
ENST00000471122.5:n.1045+95_1045+96insTGGGGTCACTCCAGAGATGGGCGGGGCCGCTCTTGGGGAGGTGGG
ENST00000485413.1:n.62+95_62+96insTGGGGTCACTCCAGAGATGGGCGGGGCCGCTCTTGGGGAGGTGGG
NM_000832.6:c.968+95_968+96insTGGGGTCACTCCAGAGATGGGCGGGGCCGCTCTTGGGGAGGTGGG NP_000823.4:n.968+95_968+96insTGGGGTCACTCCAGAGATGGGCGGGGCCGCT...
NM_001185090.1:c.1031+95_1031+96insTGGGGTCACTCCAGAGATGGGCGGGGCCGCTCTTGGGGAGGTGGG NP_001172019.1:n.1031+95_1031+96insTGGGGTCACTCCAGAGATGGGCGGGG...
NM_001185091.1:c.1031+95_1031+96insTGGGGTCACTCCAGAGATGGGCGGGGCCGCTCTTGGGGAGGTGGG NP_001172020.1:n.1031+95_1031+96insTGGGGTCACTCCAGAGATGGGCGGGG...
NM_007327.3:c.968+95_968+96insTGGGGTCACTCCAGAGATGGGCGGGGCCGCTCTTGGGGAGGTGGG NP_015566.1:n.968+95_968+96insTGGGGTCACTCCAGAGATGGGCGGGGCCGCT...
NM_021569.3:c.968+95_968+96insTGGGGTCACTCCAGAGATGGGCGGGGCCGCTCTTGGGGAGGTGGG NP_067544.1:n.968+95_968+96insTGGGGTCACTCCAGAGATGGGCGGGGCCGCT...
XM_005266071.2:c.968+95_968+96insTGGGGTCACTCCAGAGATGGGCGGGGCCGCTCTTGGGGAGGTGGG XP_005266128.1:n.968+95_968+96insTGGGGTCACTCCAGAGATGGGCGGGGCC...
XM_005266072.2:c.1031+95_1031+96insTGGGGTCACTCCAGAGATGGGCGGGGCCGCTCTTGGGGAGGTGGG XP_005266129.1:n.1031+95_1031+96insTGGGGTCACTCCAGAGATGGGCGGGG...
XM_005266073.3:c.1031+95_1031+96insTGGGGTCACTCCAGAGATGGGCGGGGCCGCTCTTGGGGAGGTGGG XP_005266130.1:n.1031+95_1031+96insTGGGGTCACTCCAGAGATGGGCGGGG...
XM_011518583.1:c.1031+95_1031+96insTGGGGTCACTCCAGAGATGGGCGGGGCCGCTCTTGGGGAGGTGGG XP_011516885.1:n.1031+95_1031+96insTGGGGTCACTCCAGAGATGGGCGGGG...
XM_005266071.3:c.968+95_968+96insTGGGGTCACTCCAGAGATGGGCGGGGCCGCTCTTGGGGAGGTGGG XP_005266128.1:n.968+95_968+96insTGGGGTCACTCCAGAGATGGGCGGGGCC...
XM_005266072.3:c.1031+95_1031+96insTGGGGTCACTCCAGAGATGGGCGGGGCCGCTCTTGGGGAGGTGGG XP_005266129.1:n.1031+95_1031+96insTGGGGTCACTCCAGAGATGGGCGGGG...
XM_005266073.4:c.1031+95_1031+96insTGGGGTCACTCCAGAGATGGGCGGGGCCGCTCTTGGGGAGGTGGG XP_005266130.1:n.1031+95_1031+96insTGGGGTCACTCCAGAGATGGGCGGGG...
XM_011518583.2:c.1031+95_1031+96insTGGGGTCACTCCAGAGATGGGCGGGGCCGCTCTTGGGGAGGTGGG XP_011516885.1:n.1031+95_1031+96insTGGGGTCACTCCAGAGATGGGCGGGG...
NM_007327.4:c.968+95_968+96insTGGGGTCACTCCAGAGATGGGCGGGGCCGCTCTTGGGGAGGTGGG MANE Select NP_015566.1:n.968+95_968+96insTGGGGTCACTCCAGAGATGGGCGGGGCCGCT...
NM_000832.7:c.968+95_968+96insTGGGGTCACTCCAGAGATGGGCGGGGCCGCTCTTGGGGAGGTGGG NP_000823.4:n.968+95_968+96insTGGGGTCACTCCAGAGATGGGCGGGGCCGCT...
NM_001185090.2:c.1031+95_1031+96insTGGGGTCACTCCAGAGATGGGCGGGGCCGCTCTTGGGGAGGTGGG NP_001172019.1:n.1031+95_1031+96insTGGGGTCACTCCAGAGATGGGCGGGG...
NM_001185091.2:c.1031+95_1031+96insTGGGGTCACTCCAGAGATGGGCGGGGCCGCTCTTGGGGAGGTGGG NP_001172020.1:n.1031+95_1031+96insTGGGGTCACTCCAGAGATGGGCGGGG...
NM_021569.4:c.968+95_968+96insTGGGGTCACTCCAGAGATGGGCGGGGCCGCTCTTGGGGAGGTGGG NP_067544.1:n.968+95_968+96insTGGGGTCACTCCAGAGATGGGCGGGGCCGCT...