Canonical Allele Identifier: CA2692779492
Gene: GRIN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137167510del , CM000671.2:g.137167510del GRCh38
NC_000009.11:g.140061962del , CM000671.1:g.140061962del GRCh37
NC_000009.10:g.139181783del NCBI36
NG_011507.1:g.33354del

Transcript Alleles

HGVS Amino-acid change
ENST00000371553.8:c.2764-264del ENSP00000360608.3:n.2764-264del
ENST00000371560.5:c.2653-264del ENSP00000360615.3:n.2653-264del
ENST00000371561.8:c.2800del MANE Select ENSP00000360616.3:p.Arg934ValfsTer?
ENST00000371546.8:c.2863del ENSP00000360601.4:p.Arg955ValfsTer?
ENST00000371550.8:c.2689del ENSP00000360605.4:p.Arg897ValfsTer?
ENST00000371553.7:c.2764-264del ENSP00000360608.3:n.2764-264del
ENST00000371555.8:c.2752del ENSP00000360610.4:p.Arg918ValfsTer?
ENST00000371559.8:c.2590-264del ENSP00000360614.4:n.2590-264del
ENST00000371560.4:c.2653-264del ENSP00000360615.3:n.2653-264del
ENST00000371561.7:c.2800del ENSP00000360616.3:p.Arg934ValfsTer?
ENST00000473811.1:n.280del
NM_000832.6:c.2590-264del NP_000823.4:n.2590-264del
NM_001185090.1:c.2764-264del NP_001172019.1:n.2764-264del
NM_001185091.1:c.2653-264del NP_001172020.1:n.2653-264del
NM_007327.3:c.2800del NP_015566.1:p.Arg934ValfsTer?
NM_021569.3:c.2689del NP_067544.1:p.Arg897ValfsTer?
XM_005266071.2:c.2701-264del XP_005266128.1:n.2701-264del
XM_005266072.2:c.2752del XP_005266129.1:p.Arg918ValfsTer?
XM_005266073.3:c.2863del XP_005266130.1:p.Arg955ValfsTer?
XM_005266071.3:c.2701-264del XP_005266128.1:n.2701-264del
XM_005266072.3:c.2752del XP_005266129.1:p.Arg918ValfsTer?
XM_005266073.4:c.2863del XP_005266130.1:p.Arg955ValfsTer?
NM_007327.4:c.2800del MANE Select NP_015566.1:p.Arg934ValfsTer?
NM_000832.7:c.2590-264del NP_000823.4:n.2590-264del
NM_001185090.2:c.2764-264del NP_001172019.1:n.2764-264del
NM_001185091.2:c.2653-264del NP_001172020.1:n.2653-264del
NM_021569.4:c.2689del NP_067544.1:p.Arg897ValfsTer?