Canonical Allele Identifier: CA1884330543
Gene: GRIN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137161704_137161706delinsGAC , CM000671.2:g.137161704_137161706delinsGAC GRCh38
NC_000009.11:g.140056156_140056158delinsGAC , CM000671.1:g.140056156_140056158delinsGAC GRCh37
NC_000009.10:g.139175977_139175979delinsGAC NCBI36
NG_011507.1:g.27548_27550delinsGAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000371553.8:c.1531-220_1531-218delinsGAC ENSP00000360608.3:n.1531-220_1531-218delinsGAC
ENST00000371560.5:c.1531-220_1531-218delinsGAC ENSP00000360615.3:n.1531-220_1531-218delinsGAC
ENST00000371561.8:c.1468-220_1468-218delinsGAC MANE Select ENSP00000360616.3:n.1468-220_1468-218delinsGAC
ENST00000675295.1:n.898-220_898-218delinsGAC
ENST00000350902.9:c.*443-220_*443-218delinsGAC ENSP00000316915.9:n.*443-220_*443-218delinsGAC
ENST00000371546.8:c.1531-220_1531-218delinsGAC ENSP00000360601.4:n.1531-220_1531-218delinsGAC
ENST00000371550.8:c.1468-220_1468-218delinsGAC ENSP00000360605.4:n.1468-220_1468-218delinsGAC
ENST00000371553.7:c.1531-220_1531-218delinsGAC ENSP00000360608.3:n.1531-220_1531-218delinsGAC
ENST00000371555.8:c.1531-220_1531-218delinsGAC ENSP00000360610.4:n.1531-220_1531-218delinsGAC
ENST00000371559.8:c.1468-220_1468-218delinsGAC ENSP00000360614.4:n.1468-220_1468-218delinsGAC
ENST00000371560.4:c.1531-220_1531-218delinsGAC ENSP00000360615.3:n.1531-220_1531-218delinsGAC
ENST00000371561.7:c.1468-220_1468-218delinsGAC ENSP00000360616.3:n.1468-220_1468-218delinsGAC
ENST00000471122.5:n.1545-220_1545-218delinsGAC
NM_000832.6:c.1468-220_1468-218delinsGAC NP_000823.4:n.1468-220_1468-218delinsGAC
NM_001185090.1:c.1531-220_1531-218delinsGAC NP_001172019.1:n.1531-220_1531-218delinsGAC
NM_001185091.1:c.1531-220_1531-218delinsGAC NP_001172020.1:n.1531-220_1531-218delinsGAC
NM_007327.3:c.1468-220_1468-218delinsGAC NP_015566.1:n.1468-220_1468-218delinsGAC
NM_021569.3:c.1468-220_1468-218delinsGAC NP_067544.1:n.1468-220_1468-218delinsGAC
XM_005266071.2:c.1468-220_1468-218delinsGAC XP_005266128.1:n.1468-220_1468-218delinsGAC
XM_005266072.2:c.1531-220_1531-218delinsGAC XP_005266129.1:n.1531-220_1531-218delinsGAC
XM_005266073.3:c.1531-220_1531-218delinsGAC XP_005266130.1:n.1531-220_1531-218delinsGAC
XM_011518583.1:c.1531-220_1531-218delinsGAC XP_011516885.1:n.1531-220_1531-218delinsGAC
XM_005266071.3:c.1468-220_1468-218delinsGAC XP_005266128.1:n.1468-220_1468-218delinsGAC
XM_005266072.3:c.1531-220_1531-218delinsGAC XP_005266129.1:n.1531-220_1531-218delinsGAC
XM_005266073.4:c.1531-220_1531-218delinsGAC XP_005266130.1:n.1531-220_1531-218delinsGAC
XM_011518583.2:c.1531-220_1531-218delinsGAC XP_011516885.1:n.1531-220_1531-218delinsGAC
NM_007327.4:c.1468-220_1468-218delinsGAC MANE Select NP_015566.1:n.1468-220_1468-218delinsGAC
NM_000832.7:c.1468-220_1468-218delinsGAC NP_000823.4:n.1468-220_1468-218delinsGAC
NM_001185090.2:c.1531-220_1531-218delinsGAC NP_001172019.1:n.1531-220_1531-218delinsGAC
NM_001185091.2:c.1531-220_1531-218delinsGAC NP_001172020.1:n.1531-220_1531-218delinsGAC
NM_021569.4:c.1468-220_1468-218delinsGAC NP_067544.1:n.1468-220_1468-218delinsGAC