Canonical Allele Identifier: CA2692776356
Gene: GRIN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137156763_137156771del , CM000671.2:g.137156763_137156771del GRCh38
NC_000009.11:g.140051215_140051223del , CM000671.1:g.140051215_140051223del GRCh37
NC_000009.10:g.139171036_139171044del NCBI36
NG_011507.1:g.22607_22615del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371553.8:c.829_837del ENSP00000360608.3:p.Gly277_Ala279del
ENST00000371560.5:c.829_837del ENSP00000360615.3:p.Gly277_Ala279del
ENST00000371561.8:c.766_774del MANE Select ENSP00000360616.3:p.Gly256_Ala258del
ENST00000675295.1:n.196_204del
ENST00000676396.1:n.2276_2284del
ENST00000350902.9:c.829_837del ENSP00000316915.9:p.Gly277_Ala279del
ENST00000371546.8:c.829_837del ENSP00000360601.4:p.Gly277_Ala279del
ENST00000371550.8:c.766_774del ENSP00000360605.4:p.Gly256_Ala258del
ENST00000371553.7:c.829_837del ENSP00000360608.3:p.Gly277_Ala279del
ENST00000371555.8:c.829_837del ENSP00000360610.4:p.Gly277_Ala279del
ENST00000371559.8:c.766_774del ENSP00000360614.4:p.Gly256_Ala258del
ENST00000371560.4:c.829_837del ENSP00000360615.3:p.Gly277_Ala279del
ENST00000371561.7:c.766_774del ENSP00000360616.3:p.Gly256_Ala258del
ENST00000471122.5:n.843_851del
NM_000832.6:c.766_774del NP_000823.4:p.Gly256_Ala258del
NM_001185090.1:c.829_837del NP_001172019.1:p.Gly277_Ala279del
NM_001185091.1:c.829_837del NP_001172020.1:p.Gly277_Ala279del
NM_007327.3:c.766_774del NP_015566.1:p.Gly256_Ala258del
NM_021569.3:c.766_774del NP_067544.1:p.Gly256_Ala258del
XM_005266071.2:c.766_774del XP_005266128.1:p.Gly256_Ala258del
XM_005266072.2:c.829_837del XP_005266129.1:p.Gly277_Ala279del
XM_005266073.3:c.829_837del XP_005266130.1:p.Gly277_Ala279del
XM_011518583.1:c.829_837del XP_011516885.1:p.Gly277_Ala279del
XM_005266071.3:c.766_774del XP_005266128.1:p.Gly256_Ala258del
XM_005266072.3:c.829_837del XP_005266129.1:p.Gly277_Ala279del
XM_005266073.4:c.829_837del XP_005266130.1:p.Gly277_Ala279del
XM_011518583.2:c.829_837del XP_011516885.1:p.Gly277_Ala279del
NM_007327.4:c.766_774del MANE Select NP_015566.1:p.Gly256_Ala258del
NM_000832.7:c.766_774del NP_000823.4:p.Gly256_Ala258del
NM_001185090.2:c.829_837del NP_001172019.1:p.Gly277_Ala279del
NM_001185091.2:c.829_837del NP_001172020.1:p.Gly277_Ala279del
NM_021569.4:c.766_774del NP_067544.1:p.Gly256_Ala258del