Canonical Allele Identifier: CA591373391
Gene: GRIN1 HGNC NCBI

Linked Data

dbSNP Id: rs1285040423

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137167416C>T , CM000671.2:g.137167416C>T GRCh38
NC_000009.11:g.140061868C>T , CM000671.1:g.140061868C>T GRCh37
NC_000009.10:g.139181689C>T NCBI36
NG_011507.1:g.33260C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371553.8:c.2764-358C>T ENSP00000360608.3:n.2764-358C>T
ENST00000371560.5:c.2653-358C>T ENSP00000360615.3:n.2653-358C>T
ENST00000371561.8:c.2706C>T MANE Select ENSP00000360616.3:p.Thr902=
ENST00000371546.8:c.2769C>T ENSP00000360601.4:p.Thr923=
ENST00000371550.8:c.2595C>T ENSP00000360605.4:p.Thr865=
ENST00000371553.7:c.2764-358C>T ENSP00000360608.3:n.2764-358C>T
ENST00000371555.8:c.2658C>T ENSP00000360610.4:p.Thr886=
ENST00000371559.8:c.2590-358C>T ENSP00000360614.4:n.2590-358C>T
ENST00000371560.4:c.2653-358C>T ENSP00000360615.3:n.2653-358C>T
ENST00000371561.7:c.2706C>T ENSP00000360616.3:p.Thr902=
ENST00000473811.1:n.186C>T
NM_000832.6:c.2590-358C>T NP_000823.4:n.2590-358C>T
NM_001185090.1:c.2764-358C>T NP_001172019.1:n.2764-358C>T
NM_001185091.1:c.2653-358C>T NP_001172020.1:n.2653-358C>T
NM_007327.3:c.2706C>T NP_015566.1:p.Thr902=
NM_021569.3:c.2595C>T NP_067544.1:p.Thr865=
XM_005266071.2:c.2701-358C>T XP_005266128.1:n.2701-358C>T
XM_005266072.2:c.2658C>T XP_005266129.1:p.Thr886=
XM_005266073.3:c.2769C>T XP_005266130.1:p.Thr923=
XM_005266071.3:c.2701-358C>T XP_005266128.1:n.2701-358C>T
XM_005266072.3:c.2658C>T XP_005266129.1:p.Thr886=
XM_005266073.4:c.2769C>T XP_005266130.1:p.Thr923=
NM_007327.4:c.2706C>T MANE Select NP_015566.1:p.Thr902=
NM_000832.7:c.2590-358C>T NP_000823.4:n.2590-358C>T
NM_001185090.2:c.2764-358C>T NP_001172019.1:n.2764-358C>T
NM_001185091.2:c.2653-358C>T NP_001172020.1:n.2653-358C>T
NM_021569.4:c.2595C>T NP_067544.1:p.Thr865=