Canonical Allele Identifier: CA1884330787
Gene: GRIN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137162076T= , CM000671.2:g.137162076T= GRCh38
NC_000009.11:g.140056528T= , CM000671.1:g.140056528T= GRCh37
NC_000009.10:g.139176349T= NCBI36
NG_011507.1:g.27920T=

Transcript Alleles

HGVS Amino-acid change
ENST00000371553.8:c.1683T= ENSP00000360608.3:p.Ile561=
ENST00000371560.5:c.1683T= ENSP00000360615.3:p.Ile561=
ENST00000371561.8:c.1620T= MANE Select ENSP00000360616.3:p.Ile540=
ENST00000675295.1:n.1050T=
ENST00000350902.9:c.*595T= ENSP00000316915.9:n.*595T=
ENST00000371546.8:c.1683T= ENSP00000360601.4:p.Ile561=
ENST00000371550.8:c.1620T= ENSP00000360605.4:p.Ile540=
ENST00000371553.7:c.1683T= ENSP00000360608.3:p.Ile561=
ENST00000371555.8:c.1683T= ENSP00000360610.4:p.Ile561=
ENST00000371559.8:c.1620T= ENSP00000360614.4:p.Ile540=
ENST00000371560.4:c.1683T= ENSP00000360615.3:p.Ile561=
ENST00000371561.7:c.1620T= ENSP00000360616.3:p.Ile540=
ENST00000471122.5:n.1697T=
NM_000832.6:c.1620T= NP_000823.4:p.Ile540=
NM_001185090.1:c.1683T= NP_001172019.1:p.Ile561=
NM_001185091.1:c.1683T= NP_001172020.1:p.Ile561=
NM_007327.3:c.1620T= NP_015566.1:p.Ile540=
NM_021569.3:c.1620T= NP_067544.1:p.Ile540=
XM_005266071.2:c.1620T= XP_005266128.1:p.Ile540=
XM_005266072.2:c.1683T= XP_005266129.1:p.Ile561=
XM_005266073.3:c.1683T= XP_005266130.1:p.Ile561=
XM_011518583.1:c.1683T= XP_011516885.1:p.Ile561=
XM_005266071.3:c.1620T= XP_005266128.1:p.Ile540=
XM_005266072.3:c.1683T= XP_005266129.1:p.Ile561=
XM_005266073.4:c.1683T= XP_005266130.1:p.Ile561=
XM_011518583.2:c.1683T= XP_011516885.1:p.Ile561=
NM_007327.4:c.1620T= MANE Select NP_015566.1:p.Ile540=
NM_000832.7:c.1620T= NP_000823.4:p.Ile540=
NM_001185090.2:c.1683T= NP_001172019.1:p.Ile561=
NM_001185091.2:c.1683T= NP_001172020.1:p.Ile561=
NM_021569.4:c.1620T= NP_067544.1:p.Ile540=