Canonical Allele Identifier: CA5360657
Gene: GRIN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 389124
dbSNP Id: rs201424528

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137145758G>A , CM000671.2:g.137145758G>A GRCh38
NC_000009.11:g.140040210G>A , CM000671.1:g.140040210G>A GRCh37
NC_000009.10:g.139160031G>A NCBI36
NG_011507.1:g.11602G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371553.8:c.426G>A ENSP00000360608.3:p.Pro142=
ENST00000371560.5:c.426G>A ENSP00000360615.3:p.Pro142=
ENST00000371561.8:c.426G>A MANE Select ENSP00000360616.3:p.Pro142=
ENST00000350902.9:c.426G>A ENSP00000316915.9:p.Pro142=
ENST00000371546.8:c.426G>A ENSP00000360601.4:p.Pro142=
ENST00000371550.8:c.426G>A ENSP00000360605.4:p.Pro142=
ENST00000371553.7:c.426G>A ENSP00000360608.3:p.Pro142=
ENST00000371555.8:c.426G>A ENSP00000360610.4:p.Pro142=
ENST00000371559.8:c.426G>A ENSP00000360614.4:p.Pro142=
ENST00000371560.4:c.426G>A ENSP00000360615.3:p.Pro142=
ENST00000371561.7:c.426G>A ENSP00000360616.3:p.Pro142=
ENST00000471122.5:n.503G>A
NM_000832.6:c.426G>A NP_000823.4:p.Pro142=
NM_001185090.1:c.426G>A NP_001172019.1:p.Pro142=
NM_001185091.1:c.426G>A NP_001172020.1:p.Pro142=
NM_007327.3:c.426G>A NP_015566.1:p.Pro142=
NM_021569.3:c.426G>A NP_067544.1:p.Pro142=
XM_005266071.2:c.426G>A XP_005266128.1:p.Pro142=
XM_005266072.2:c.426G>A XP_005266129.1:p.Pro142=
XM_005266073.3:c.426G>A XP_005266130.1:p.Pro142=
XM_011518583.1:c.426G>A XP_011516885.1:p.Pro142=
XM_005266071.3:c.426G>A XP_005266128.1:p.Pro142=
XM_005266072.3:c.426G>A XP_005266129.1:p.Pro142=
XM_005266073.4:c.426G>A XP_005266130.1:p.Pro142=
XM_011518583.2:c.426G>A XP_011516885.1:p.Pro142=
NM_007327.4:c.426G>A MANE Select NP_015566.1:p.Pro142=
NM_000832.7:c.426G>A NP_000823.4:p.Pro142=
NM_001185090.2:c.426G>A NP_001172019.1:p.Pro142=
NM_001185091.2:c.426G>A NP_001172020.1:p.Pro142=
NM_021569.4:c.426G>A NP_067544.1:p.Pro142=