Canonical Allele Identifier: CA15993074
Gene: GRIK1 HGNC NCBI
dbSNP:
458685
gnomAD v2:
21:31177511 A / G
gnomAD v3:
21:29805194 A / G
gnomAD v4:
chr21-29805194-A-G
Joint Max Group AF 0.16110733 (NFE)
Genomes Max Group AF 0.16110733 (NFE)
MyVariant.info:
GRCh38 chr21:g.29805194A>G
GRCh37 chr21:g.31177511A>G
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.29805194A>G , CM000683.2:g.29805194A>G GRCh38
NC_000021.8:g.31177511A>G , CM000683.1:g.31177511A>G GRCh37
NC_000021.7:g.30099382A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000399907.6:c.119-111131T>C ENSP00000382791.1:n.119-111131T>C
ENST00000327783.9:c.119-111131T>C MANE Select ENSP00000327687.4:n.119-111131T>C
ENST00000327783.8:c.119-111131T>C ENSP00000327687.4:n.119-111131T>C
ENST00000389124.6:c.119-111131T>C ENSP00000373776.2:n.119-111131T>C
ENST00000389125.7:c.119-111131T>C ENSP00000373777.3:n.119-111131T>C
ENST00000399907.5:c.119-111131T>C ENSP00000382791.1:n.119-111131T>C
ENST00000399909.5:c.119-111131T>C ENSP00000382793.1:n.119-111131T>C
ENST00000399913.5:c.119-111131T>C ENSP00000382797.1:n.119-111131T>C
ENST00000399914.5:c.119-111131T>C ENSP00000382798.1:n.119-111131T>C
ENST00000472429.1:n.652-111131T>C
NM_000830.3:c.119-111131T>C NP_000821.1:n.119-111131T>C
NM_175611.2:c.119-111131T>C NP_783300.1:n.119-111131T>C
XM_005260942.1:c.119-111131T>C XP_005260999.1:n.119-111131T>C
XM_005260943.1:c.119-111131T>C XP_005261000.1:n.119-111131T>C
XM_005260944.2:c.119-111131T>C XP_005261001.1:n.119-111131T>C
XM_006723991.1:c.119-111131T>C XP_006724054.1:n.119-111131T>C
XM_011529527.1:c.119-111131T>C XP_011527829.1:n.119-111131T>C
XM_011529528.1:c.119-111131T>C XP_011527830.1:n.119-111131T>C
NM_000830.4:c.119-111131T>C NP_000821.1:n.119-111131T>C
NM_001320616.1:c.119-111131T>C NP_001307545.1:n.119-111131T>C
NM_001320618.1:c.119-115209T>C NP_001307547.1:n.119-115209T>C
NM_001320621.1:c.119-132030T>C NP_001307550.1:n.119-132030T>C
NM_001320630.1:c.119-111131T>C NP_001307559.1:n.119-111131T>C
NM_001330993.1:c.119-111131T>C NP_001317922.1:n.119-111131T>C
NM_001330994.1:c.119-111131T>C NP_001317923.1:n.119-111131T>C
XM_005260944.3:c.119-111131T>C XP_005261001.1:n.119-111131T>C
XR_001754829.2:n.289-111131T>C
NM_000830.5:c.119-111131T>C NP_000821.1:n.119-111131T>C
NM_001320616.2:c.119-111131T>C NP_001307545.1:n.119-111131T>C
NM_001320618.2:c.119-115209T>C NP_001307547.1:n.119-115209T>C
NM_001320621.2:c.119-132030T>C NP_001307550.1:n.119-132030T>C
NM_001330993.2:c.119-111131T>C NP_001317922.1:n.119-111131T>C
NM_001330994.2:c.119-111131T>C MANE Select NP_001317923.1:n.119-111131T>C
NM_175611.3:c.119-111131T>C NP_783300.1:n.119-111131T>C
NM_000830.6:c.119-111131T>C NP_000821.1:n.119-111131T>C
NM_001320630.2:c.119-111131T>C NP_001307559.1:n.119-111131T>C
NM_001393424.1:c.119-111131T>C NP_001380353.1:n.119-111131T>C
NM_001393425.1:c.119-111131T>C NP_001380354.1:n.119-111131T>C
NM_001393426.1:c.119-115209T>C NP_001380355.1:n.119-115209T>C
Search 100 bp 5'
Search 100 bp 3'