Canonical Allele Identifier: CA467777143
Gene: GRIN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1088878
ClinVar RCV Id: RCV001407525
dbSNP Id: rs1468821601

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137161944G>A , CM000671.2:g.137161944G>A GRCh38
NC_000009.11:g.140056396G>A , CM000671.1:g.140056396G>A GRCh37
NC_000009.10:g.139176217G>A NCBI36
NG_011507.1:g.27788G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371553.8:c.1551G>A ENSP00000360608.3:p.Lys517=
ENST00000371560.5:c.1551G>A ENSP00000360615.3:p.Lys517=
ENST00000371561.8:c.1488G>A MANE Select ENSP00000360616.3:p.Lys496=
ENST00000675295.1:n.918G>A
ENST00000350902.9:c.*463G>A ENSP00000316915.9:n.*463G>A
ENST00000371546.8:c.1551G>A ENSP00000360601.4:p.Lys517=
ENST00000371550.8:c.1488G>A ENSP00000360605.4:p.Lys496=
ENST00000371553.7:c.1551G>A ENSP00000360608.3:p.Lys517=
ENST00000371555.8:c.1551G>A ENSP00000360610.4:p.Lys517=
ENST00000371559.8:c.1488G>A ENSP00000360614.4:p.Lys496=
ENST00000371560.4:c.1551G>A ENSP00000360615.3:p.Lys517=
ENST00000371561.7:c.1488G>A ENSP00000360616.3:p.Lys496=
ENST00000471122.5:n.1565G>A
NM_000832.6:c.1488G>A NP_000823.4:p.Lys496=
NM_001185090.1:c.1551G>A NP_001172019.1:p.Lys517=
NM_001185091.1:c.1551G>A NP_001172020.1:p.Lys517=
NM_007327.3:c.1488G>A NP_015566.1:p.Lys496=
NM_021569.3:c.1488G>A NP_067544.1:p.Lys496=
XM_005266071.2:c.1488G>A XP_005266128.1:p.Lys496=
XM_005266072.2:c.1551G>A XP_005266129.1:p.Lys517=
XM_005266073.3:c.1551G>A XP_005266130.1:p.Lys517=
XM_011518583.1:c.1551G>A XP_011516885.1:p.Lys517=
XM_005266071.3:c.1488G>A XP_005266128.1:p.Lys496=
XM_005266072.3:c.1551G>A XP_005266129.1:p.Lys517=
XM_005266073.4:c.1551G>A XP_005266130.1:p.Lys517=
XM_011518583.2:c.1551G>A XP_011516885.1:p.Lys517=
NM_007327.4:c.1488G>A MANE Select NP_015566.1:p.Lys496=
NM_000832.7:c.1488G>A NP_000823.4:p.Lys496=
NM_001185090.2:c.1551G>A NP_001172019.1:p.Lys517=
NM_001185091.2:c.1551G>A NP_001172020.1:p.Lys517=
NM_021569.4:c.1488G>A NP_067544.1:p.Lys496=