Canonical Allele Identifier: CA1884318350
Gene: GRIN1 HGNC NCBI

Linked Data

dbSNP Id: rs1832041911

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137139403_137139404del , CM000671.2:g.137139403_137139404del GRCh38
NC_000009.11:g.140033855_140033856del , CM000671.1:g.140033855_140033856del GRCh37
NC_000009.10:g.139153676_139153677del NCBI36
NG_011507.1:g.5247_5248del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371553.8:c.-84_-83del ENSP00000360608.3:n.-84_-83del
ENST00000371560.5:c.-84_-83del ENSP00000360615.3:n.-84_-83del
ENST00000371561.8:c.-84_-83del MANE Select ENSP00000360616.3:n.-84_-83del
ENST00000350902.9:c.-84_-83del ENSP00000316915.9:n.-84_-83del
ENST00000371561.7:c.-84_-83del ENSP00000360616.3:n.-84_-83del
NM_000832.6:c.-84_-83del NP_000823.4:n.-84_-83del
NM_001185090.1:c.-84_-83del NP_001172019.1:n.-84_-83del
NM_001185091.1:c.-84_-83del NP_001172020.1:n.-84_-83del
NM_007327.3:c.-84_-83del NP_015566.1:n.-84_-83del
NM_021569.3:c.-84_-83del NP_067544.1:n.-84_-83del
XM_005266071.2:c.-84_-83del XP_005266128.1:n.-84_-83del
XM_005266072.2:c.-84_-83del XP_005266129.1:n.-84_-83del
XM_005266073.3:c.-84_-83del XP_005266130.1:n.-84_-83del
XM_011518583.1:c.-84_-83del XP_011516885.1:n.-84_-83del
XM_005266072.3:c.-84_-83del XP_005266129.1:n.-84_-83del
XM_005266073.4:c.-84_-83del XP_005266130.1:n.-84_-83del
XM_011518583.2:c.-84_-83del XP_011516885.1:n.-84_-83del
NM_007327.4:c.-84_-83del MANE Select NP_015566.1:n.-84_-83del
NM_000832.7:c.-84_-83del NP_000823.4:n.-84_-83del
NM_001185090.2:c.-84_-83del NP_001172019.1:n.-84_-83del
NM_001185091.2:c.-84_-83del NP_001172020.1:n.-84_-83del
NM_021569.4:c.-84_-83del NP_067544.1:n.-84_-83del