Canonical Allele Identifier: CA375722795
Gene: GRIN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137163183T>G , CM000671.2:g.137163183T>G GRCh38
NC_000009.11:g.140057635T>G , CM000671.1:g.140057635T>G GRCh37
NC_000009.10:g.139177456T>G NCBI36
NG_011507.1:g.29027T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371553.8:c.2249T>G ENSP00000360608.3:p.Phe750Cys
ENST00000371560.5:c.2249T>G ENSP00000360615.3:p.Phe750Cys
ENST00000371561.8:c.2186T>G MANE Select ENSP00000360616.3:p.Phe729Cys
ENST00000675295.1:n.1616T>G
ENST00000350902.9:c.*1161T>G ENSP00000316915.9:n.*1161T>G
ENST00000371546.8:c.2249T>G ENSP00000360601.4:p.Phe750Cys
ENST00000371550.8:c.2186T>G ENSP00000360605.4:p.Phe729Cys
ENST00000371553.7:c.2249T>G ENSP00000360608.3:p.Phe750Cys
ENST00000371555.8:c.2249T>G ENSP00000360610.4:p.Phe750Cys
ENST00000371559.8:c.2186T>G ENSP00000360614.4:p.Phe729Cys
ENST00000371560.4:c.2249T>G ENSP00000360615.3:p.Phe750Cys
ENST00000371561.7:c.2186T>G ENSP00000360616.3:p.Phe729Cys
ENST00000460273.1:n.207T>G
ENST00000471122.5:n.2263T>G
NM_000832.6:c.2186T>G NP_000823.4:p.Phe729Cys
NM_001185090.1:c.2249T>G NP_001172019.1:p.Phe750Cys
NM_001185091.1:c.2249T>G NP_001172020.1:p.Phe750Cys
NM_007327.3:c.2186T>G NP_015566.1:p.Phe729Cys
NM_021569.3:c.2186T>G NP_067544.1:p.Phe729Cys
XM_005266071.2:c.2186T>G XP_005266128.1:p.Phe729Cys
XM_005266072.2:c.2249T>G XP_005266129.1:p.Phe750Cys
XM_005266073.3:c.2249T>G XP_005266130.1:p.Phe750Cys
XM_011518583.1:c.2249T>G XP_011516885.1:p.Phe750Cys
XM_005266071.3:c.2186T>G XP_005266128.1:p.Phe729Cys
XM_005266072.3:c.2249T>G XP_005266129.1:p.Phe750Cys
XM_005266073.4:c.2249T>G XP_005266130.1:p.Phe750Cys
XM_011518583.2:c.2249T>G XP_011516885.1:p.Phe750Cys
NM_007327.4:c.2186T>G MANE Select NP_015566.1:p.Phe729Cys
NM_000832.7:c.2186T>G NP_000823.4:p.Phe729Cys
NM_001185090.2:c.2249T>G NP_001172019.1:p.Phe750Cys
NM_001185091.2:c.2249T>G NP_001172020.1:p.Phe750Cys
NM_021569.4:c.2186T>G NP_067544.1:p.Phe729Cys