Canonical Allele Identifier: CA2579529048
Gene: GRIN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137167421del , CM000671.2:g.137167421del GRCh38
NC_000009.11:g.140061873del , CM000671.1:g.140061873del GRCh37
NC_000009.10:g.139181694del NCBI36
NG_011507.1:g.33265del

Transcript Alleles

HGVS Amino-acid change
ENST00000371553.8:c.2764-353del ENSP00000360608.3:n.2764-353del
ENST00000371560.5:c.2653-353del ENSP00000360615.3:n.2653-353del
ENST00000371561.8:c.2711del MANE Select ENSP00000360616.3:p.Gly904ValfsTer?
ENST00000371546.8:c.2774del ENSP00000360601.4:p.Gly925ValfsTer?
ENST00000371550.8:c.2600del ENSP00000360605.4:p.Gly867ValfsTer?
ENST00000371553.7:c.2764-353del ENSP00000360608.3:n.2764-353del
ENST00000371555.8:c.2663del ENSP00000360610.4:p.Gly888ValfsTer?
ENST00000371559.8:c.2590-353del ENSP00000360614.4:n.2590-353del
ENST00000371560.4:c.2653-353del ENSP00000360615.3:n.2653-353del
ENST00000371561.7:c.2711del ENSP00000360616.3:p.Gly904ValfsTer?
ENST00000473811.1:n.191del
NM_000832.6:c.2590-353del NP_000823.4:n.2590-353del
NM_001185090.1:c.2764-353del NP_001172019.1:n.2764-353del
NM_001185091.1:c.2653-353del NP_001172020.1:n.2653-353del
NM_007327.3:c.2711del NP_015566.1:p.Gly904ValfsTer?
NM_021569.3:c.2600del NP_067544.1:p.Gly867ValfsTer?
XM_005266071.2:c.2701-353del XP_005266128.1:n.2701-353del
XM_005266072.2:c.2663del XP_005266129.1:p.Gly888ValfsTer?
XM_005266073.3:c.2774del XP_005266130.1:p.Gly925ValfsTer?
XM_005266071.3:c.2701-353del XP_005266128.1:n.2701-353del
XM_005266072.3:c.2663del XP_005266129.1:p.Gly888ValfsTer?
XM_005266073.4:c.2774del XP_005266130.1:p.Gly925ValfsTer?
NM_007327.4:c.2711del MANE Select NP_015566.1:p.Gly904ValfsTer?
NM_000832.7:c.2590-353del NP_000823.4:n.2590-353del
NM_001185090.2:c.2764-353del NP_001172019.1:n.2764-353del
NM_001185091.2:c.2653-353del NP_001172020.1:n.2653-353del
NM_021569.4:c.2600del NP_067544.1:p.Gly867ValfsTer?