Canonical Allele Identifier: CA1884331059
Gene: GRIN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137162802_137162803delinsGC , CM000671.2:g.137162802_137162803delinsGC GRCh38
NC_000009.11:g.140057254_140057255delinsGC , CM000671.1:g.140057254_140057255delinsGC GRCh37
NC_000009.10:g.139177075_139177076delinsGC NCBI36
NG_011507.1:g.28646_28647delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000371553.8:c.2077-44_2077-43delinsGC ENSP00000360608.3:n.2077-44_2077-43delinsGC
ENST00000371560.5:c.2077-44_2077-43delinsGC ENSP00000360615.3:n.2077-44_2077-43delinsGC
ENST00000371561.8:c.2014-44_2014-43delinsGC MANE Select ENSP00000360616.3:n.2014-44_2014-43delinsGC
ENST00000675295.1:n.1444-44_1444-43delinsGC
ENST00000350902.9:c.*989-44_*989-43delinsGC ENSP00000316915.9:n.*989-44_*989-43delinsGC
ENST00000371546.8:c.2077-44_2077-43delinsGC ENSP00000360601.4:n.2077-44_2077-43delinsGC
ENST00000371550.8:c.2014-44_2014-43delinsGC ENSP00000360605.4:n.2014-44_2014-43delinsGC
ENST00000371553.7:c.2077-44_2077-43delinsGC ENSP00000360608.3:n.2077-44_2077-43delinsGC
ENST00000371555.8:c.2077-44_2077-43delinsGC ENSP00000360610.4:n.2077-44_2077-43delinsGC
ENST00000371559.8:c.2014-44_2014-43delinsGC ENSP00000360614.4:n.2014-44_2014-43delinsGC
ENST00000371560.4:c.2077-44_2077-43delinsGC ENSP00000360615.3:n.2077-44_2077-43delinsGC
ENST00000371561.7:c.2014-44_2014-43delinsGC ENSP00000360616.3:n.2014-44_2014-43delinsGC
ENST00000460273.1:n.35-44_35-43delinsGC
ENST00000471122.5:n.2091-44_2091-43delinsGC
NM_000832.6:c.2014-44_2014-43delinsGC NP_000823.4:n.2014-44_2014-43delinsGC
NM_001185090.1:c.2077-44_2077-43delinsGC NP_001172019.1:n.2077-44_2077-43delinsGC
NM_001185091.1:c.2077-44_2077-43delinsGC NP_001172020.1:n.2077-44_2077-43delinsGC
NM_007327.3:c.2014-44_2014-43delinsGC NP_015566.1:n.2014-44_2014-43delinsGC
NM_021569.3:c.2014-44_2014-43delinsGC NP_067544.1:n.2014-44_2014-43delinsGC
XM_005266071.2:c.2014-44_2014-43delinsGC XP_005266128.1:n.2014-44_2014-43delinsGC
XM_005266072.2:c.2077-44_2077-43delinsGC XP_005266129.1:n.2077-44_2077-43delinsGC
XM_005266073.3:c.2077-44_2077-43delinsGC XP_005266130.1:n.2077-44_2077-43delinsGC
XM_011518583.1:c.2077-44_2077-43delinsGC XP_011516885.1:n.2077-44_2077-43delinsGC
XM_005266071.3:c.2014-44_2014-43delinsGC XP_005266128.1:n.2014-44_2014-43delinsGC
XM_005266072.3:c.2077-44_2077-43delinsGC XP_005266129.1:n.2077-44_2077-43delinsGC
XM_005266073.4:c.2077-44_2077-43delinsGC XP_005266130.1:n.2077-44_2077-43delinsGC
XM_011518583.2:c.2077-44_2077-43delinsGC XP_011516885.1:n.2077-44_2077-43delinsGC
NM_007327.4:c.2014-44_2014-43delinsGC MANE Select NP_015566.1:n.2014-44_2014-43delinsGC
NM_000832.7:c.2014-44_2014-43delinsGC NP_000823.4:n.2014-44_2014-43delinsGC
NM_001185090.2:c.2077-44_2077-43delinsGC NP_001172019.1:n.2077-44_2077-43delinsGC
NM_001185091.2:c.2077-44_2077-43delinsGC NP_001172020.1:n.2077-44_2077-43delinsGC
NM_021569.4:c.2014-44_2014-43delinsGC NP_067544.1:n.2014-44_2014-43delinsGC