Canonical Allele Identifier: CA2579528618
Gene: GRIN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137157038del , CM000671.2:g.137157038del GRCh38
NC_000009.11:g.140051490del , CM000671.1:g.140051490del GRCh37
NC_000009.10:g.139171311del NCBI36
NG_011507.1:g.22882del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371553.8:c.1031+1del
ENST00000371560.5:c.1031+1del
ENST00000371561.8:c.968+1del
ENST00000675295.1:n.398+1del
ENST00000676396.1:n.2478+1del
ENST00000350902.9:c.1014+1del
ENST00000371546.8:c.1031+1del
ENST00000371550.8:c.968+1del
ENST00000371553.7:c.1031+1del
ENST00000371555.8:c.1031+1del
ENST00000371559.8:c.968+1del
ENST00000371560.4:c.1031+1del
ENST00000371561.7:c.968+1del
ENST00000471122.5:n.1045+1del
ENST00000485413.1:n.62+1del
NM_000832.6:c.968+1del
NM_001185090.1:c.1031+1del
NM_001185091.1:c.1031+1del
NM_007327.3:c.968+1del
NM_021569.3:c.968+1del
XM_005266071.2:c.968+1del
XM_005266072.2:c.1031+1del
XM_005266073.3:c.1031+1del
XM_011518583.1:c.1031+1del
XM_005266071.3:c.968+1del
XM_005266072.3:c.1031+1del
XM_005266073.4:c.1031+1del
XM_011518583.2:c.1031+1del
NM_007327.4:c.968+1del
NM_000832.7:c.968+1del
NM_001185090.2:c.1031+1del
NM_001185091.2:c.1031+1del
NM_021569.4:c.968+1del