Canonical Allele Identifier: CA375729585
Gene: GRIN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137167424G>T , CM000671.2:g.137167424G>T GRCh38
NC_000009.11:g.140061876G>T , CM000671.1:g.140061876G>T GRCh37
NC_000009.10:g.139181697G>T NCBI36
NG_011507.1:g.33268G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371553.8:c.2764-350G>T ENSP00000360608.3:n.2764-350G>T
ENST00000371560.5:c.2653-350G>T ENSP00000360615.3:n.2653-350G>T
ENST00000371561.8:c.2714G>T MANE Select ENSP00000360616.3:p.Gly905Val
ENST00000371546.8:c.2777G>T ENSP00000360601.4:p.Gly926Val
ENST00000371550.8:c.2603G>T ENSP00000360605.4:p.Gly868Val
ENST00000371553.7:c.2764-350G>T ENSP00000360608.3:n.2764-350G>T
ENST00000371555.8:c.2666G>T ENSP00000360610.4:p.Gly889Val
ENST00000371559.8:c.2590-350G>T ENSP00000360614.4:n.2590-350G>T
ENST00000371560.4:c.2653-350G>T ENSP00000360615.3:n.2653-350G>T
ENST00000371561.7:c.2714G>T ENSP00000360616.3:p.Gly905Val
ENST00000473811.1:n.194G>T
NM_000832.6:c.2590-350G>T NP_000823.4:n.2590-350G>T
NM_001185090.1:c.2764-350G>T NP_001172019.1:n.2764-350G>T
NM_001185091.1:c.2653-350G>T NP_001172020.1:n.2653-350G>T
NM_007327.3:c.2714G>T NP_015566.1:p.Gly905Val
NM_021569.3:c.2603G>T NP_067544.1:p.Gly868Val
XM_005266071.2:c.2701-350G>T XP_005266128.1:n.2701-350G>T
XM_005266072.2:c.2666G>T XP_005266129.1:p.Gly889Val
XM_005266073.3:c.2777G>T XP_005266130.1:p.Gly926Val
XM_005266071.3:c.2701-350G>T XP_005266128.1:n.2701-350G>T
XM_005266072.3:c.2666G>T XP_005266129.1:p.Gly889Val
XM_005266073.4:c.2777G>T XP_005266130.1:p.Gly926Val
NM_007327.4:c.2714G>T MANE Select NP_015566.1:p.Gly905Val
NM_000832.7:c.2590-350G>T NP_000823.4:n.2590-350G>T
NM_001185090.2:c.2764-350G>T NP_001172019.1:n.2764-350G>T
NM_001185091.2:c.2653-350G>T NP_001172020.1:n.2653-350G>T
NM_021569.4:c.2603G>T NP_067544.1:p.Gly868Val