Canonical Allele Identifier: CA15981882
Gene: GRIK1 HGNC NCBI

Linked Data

dbSNP Id: rs2832407

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.29595188C>A , CM000683.2:g.29595188C>A GRCh38
NC_000021.8:g.30967508C>A , CM000683.1:g.30967508C>A GRCh37
NC_000021.7:g.29889379C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000327783.9:c.1251+1338G>T MANE Select ENSP00000327687.4:p.=
ENST00000309434.8:n.1134+1338G>T ENSP00000311646.8:p.=
ENST00000327783.8:c.1251+1338G>T ENSP00000327687.4:p.=
ENST00000389124.6:c.1251+1338G>T ENSP00000373776.2:p.=
ENST00000389125.7:c.1206+3642G>T ENSP00000373777.3:p.=
ENST00000399907.5:c.1251+1338G>T ENSP00000382791.1:p.=
ENST00000399909.5:c.1206+3642G>T ENSP00000382793.1:p.=
ENST00000399913.5:c.1251+1338G>T ENSP00000382797.1:p.=
ENST00000399914.5:c.1206+3642G>T ENSP00000382798.1:p.=
ENST00000422809.5:n.513-2382C>A
ENST00000468059.1:n.326-2382C>A
ENST00000535441.5:n.1089+3642G>T ENSP00000446326.2:p.=
NM_000830.3:c.1251+1338G>T NP_000821.1:p.=
NM_175611.2:c.1206+3642G>T NP_783300.1:p.=
XM_005260942.1:c.1206+3642G>T XP_005260999.1:p.=
XM_005260943.1:c.1251+1338G>T XP_005261000.1:p.=
XM_005260944.2:c.1206+3642G>T XP_005261001.1:p.=
XM_006723991.1:c.1251+1338G>T XP_006724054.1:p.=
XM_011529527.1:c.1251+1338G>T XP_011527829.1:p.=
XM_011529528.1:c.1251+1338G>T XP_011527830.1:p.=
NM_000830.4:c.1251+1338G>T NP_000821.1:p.=
NM_001320616.1:c.1251+1338G>T NP_001307545.1:p.=
NM_001320618.1:c.1038+3642G>T NP_001307547.1:p.=
NM_001320621.1:c.780+3642G>T NP_001307550.1:p.=
NM_001330993.1:c.1206+3642G>T NP_001317922.1:p.=
NM_001330994.1:c.1251+1338G>T NP_001317923.1:p.=
XM_005260944.3:c.1206+3642G>T XP_005261001.1:p.=
XR_001754829.2:n.1421+1338G>T
NM_000830.5:c.1251+1338G>T NP_000821.1:p.=
NM_001320616.2:c.1251+1338G>T NP_001307545.1:p.=
NM_001320618.2:c.1038+3642G>T NP_001307547.1:p.=
NM_001320621.2:c.780+3642G>T NP_001307550.1:p.=
NM_001330993.2:c.1206+3642G>T NP_001317922.1:p.=
NM_001330994.2:c.1251+1338G>T MANE Select NP_001317923.1:p.=
NM_175611.3:c.1206+3642G>T NP_783300.1:p.=
NM_000830.6:c.1251+1338G>T NP_000821.1:p.=
NM_001393424.1:c.1206+3642G>T NP_001380353.1:p.=
NM_001393425.1:c.1251+1338G>T NP_001380354.1:p.=
NM_001393426.1:c.1083+1338G>T NP_001380355.1:p.=