Canonical Allele Identifier: CA2954063133
Gene: GRIN1 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000371553.8:c.2764-353dup ENSP00000360608.3:n.2764-353dup
ENST00000371560.5:c.2653-353dup ENSP00000360615.3:n.2653-353dup
ENST00000371561.8:c.2711dup MANE Select ENSP00000360616.3:p.Gly905TrpfsTer19
ENST00000371546.8:c.2774dup ENSP00000360601.4:p.Gly926TrpfsTer19
ENST00000371550.8:c.2600dup ENSP00000360605.4:p.Gly868TrpfsTer19
ENST00000371553.7:c.2764-353dup ENSP00000360608.3:n.2764-353dup
ENST00000371555.8:c.2663dup ENSP00000360610.4:p.Gly889TrpfsTer19
ENST00000371559.8:c.2590-353dup ENSP00000360614.4:n.2590-353dup
ENST00000371560.4:c.2653-353dup ENSP00000360615.3:n.2653-353dup
ENST00000371561.7:c.2711dup ENSP00000360616.3:p.Gly905TrpfsTer19
ENST00000473811.1:n.191dup
NM_000832.6:c.2590-353dup NP_000823.4:n.2590-353dup
NM_001185090.1:c.2764-353dup NP_001172019.1:n.2764-353dup
NM_001185091.1:c.2653-353dup NP_001172020.1:n.2653-353dup
NM_007327.3:c.2711dup NP_015566.1:p.Gly905TrpfsTer19
NM_021569.3:c.2600dup NP_067544.1:p.Gly868TrpfsTer19
XM_005266071.2:c.2701-353dup XP_005266128.1:n.2701-353dup
XM_005266072.2:c.2663dup XP_005266129.1:p.Gly889TrpfsTer19
XM_005266073.3:c.2774dup XP_005266130.1:p.Gly926TrpfsTer19
XM_005266071.3:c.2701-353dup XP_005266128.1:n.2701-353dup
XM_005266072.3:c.2663dup XP_005266129.1:p.Gly889TrpfsTer19
XM_005266073.4:c.2774dup XP_005266130.1:p.Gly926TrpfsTer19
NM_007327.4:c.2711dup MANE Select NP_015566.1:p.Gly905TrpfsTer19
NM_000832.7:c.2590-353dup NP_000823.4:n.2590-353dup
NM_001185090.2:c.2764-353dup NP_001172019.1:n.2764-353dup
NM_001185091.2:c.2653-353dup NP_001172020.1:n.2653-353dup
NM_021569.4:c.2600dup NP_067544.1:p.Gly868TrpfsTer19