Canonical Allele Identifier: CA1884328136
Gene: GRIN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137156959A= , CM000671.2:g.137156959A= GRCh38
NC_000009.11:g.140051411A= , CM000671.1:g.140051411A= GRCh37
NC_000009.10:g.139171232A= NCBI36
NG_011507.1:g.22803A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371553.8:c.953A= ENSP00000360608.3:p.Glu318=
ENST00000371560.5:c.953A= ENSP00000360615.3:p.Glu318=
ENST00000371561.8:c.890A= MANE Select ENSP00000360616.3:p.Glu297=
ENST00000675295.1:n.320A=
ENST00000676396.1:n.2400A=
ENST00000350902.9:c.936A= ENSP00000316915.9:p.Arg312=
ENST00000371546.8:c.953A= ENSP00000360601.4:p.Glu318=
ENST00000371550.8:c.890A= ENSP00000360605.4:p.Glu297=
ENST00000371553.7:c.953A= ENSP00000360608.3:p.Glu318=
ENST00000371555.8:c.953A= ENSP00000360610.4:p.Glu318=
ENST00000371559.8:c.890A= ENSP00000360614.4:p.Glu297=
ENST00000371560.4:c.953A= ENSP00000360615.3:p.Glu318=
ENST00000371561.7:c.890A= ENSP00000360616.3:p.Glu297=
ENST00000471122.5:n.967A=
NM_000832.6:c.890A= NP_000823.4:p.Glu297=
NM_001185090.1:c.953A= NP_001172019.1:p.Glu318=
NM_001185091.1:c.953A= NP_001172020.1:p.Glu318=
NM_007327.3:c.890A= NP_015566.1:p.Glu297=
NM_021569.3:c.890A= NP_067544.1:p.Glu297=
XM_005266071.2:c.890A= XP_005266128.1:p.Glu297=
XM_005266072.2:c.953A= XP_005266129.1:p.Glu318=
XM_005266073.3:c.953A= XP_005266130.1:p.Glu318=
XM_011518583.1:c.953A= XP_011516885.1:p.Glu318=
XM_005266071.3:c.890A= XP_005266128.1:p.Glu297=
XM_005266072.3:c.953A= XP_005266129.1:p.Glu318=
XM_005266073.4:c.953A= XP_005266130.1:p.Glu318=
XM_011518583.2:c.953A= XP_011516885.1:p.Glu318=
NM_007327.4:c.890A= MANE Select NP_015566.1:p.Glu297=
NM_000832.7:c.890A= NP_000823.4:p.Glu297=
NM_001185090.2:c.953A= NP_001172019.1:p.Glu318=
NM_001185091.2:c.953A= NP_001172020.1:p.Glu318=
NM_021569.4:c.890A= NP_067544.1:p.Glu297=