Canonical Allele Identifier: CA15981888
Gene: GRIK1 HGNC NCBI
dbSNP:
gnomAD v4:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.29872161C>T , CM000683.2:g.29872161C>T GRCh38
NC_000021.8:g.31244478C>T , CM000683.1:g.31244478C>T GRCh37
NC_000021.7:g.30166349C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000399907.6:c.118+67222G>A ENSP00000382791.1:n.118+67222G>A
ENST00000327783.9:c.118+67222G>A MANE Select ENSP00000327687.4:n.118+67222G>A
ENST00000327783.8:c.118+67222G>A ENSP00000327687.4:n.118+67222G>A
ENST00000389124.6:c.118+67222G>A ENSP00000373776.2:n.118+67222G>A
ENST00000389125.7:c.118+67222G>A ENSP00000373777.3:n.118+67222G>A
ENST00000399907.5:c.118+67222G>A ENSP00000382791.1:n.118+67222G>A
ENST00000399909.5:c.118+67222G>A ENSP00000382793.1:n.118+67222G>A
ENST00000399913.5:c.118+67222G>A ENSP00000382797.1:n.118+67222G>A
ENST00000399914.5:c.118+67222G>A ENSP00000382798.1:n.118+67222G>A
ENST00000472429.1:n.651+67222G>A
NM_000830.3:c.118+67222G>A NP_000821.1:n.118+67222G>A
NM_175611.2:c.118+67222G>A NP_783300.1:n.118+67222G>A
XM_005260942.1:c.118+67222G>A XP_005260999.1:n.118+67222G>A
XM_005260943.1:c.118+67222G>A XP_005261000.1:n.118+67222G>A
XM_005260944.2:c.118+67222G>A XP_005261001.1:n.118+67222G>A
XM_006723991.1:c.118+67222G>A XP_006724054.1:n.118+67222G>A
XM_011529527.1:c.118+67222G>A XP_011527829.1:n.118+67222G>A
XM_011529528.1:c.118+67222G>A XP_011527830.1:n.118+67222G>A
NM_000830.4:c.118+67222G>A NP_000821.1:n.118+67222G>A
NM_001320616.1:c.118+67222G>A NP_001307545.1:n.118+67222G>A
NM_001320618.1:c.118+67222G>A NP_001307547.1:n.118+67222G>A
NM_001320621.1:c.118+67222G>A NP_001307550.1:n.118+67222G>A
NM_001320630.1:c.118+67222G>A NP_001307559.1:n.118+67222G>A
NM_001330993.1:c.118+67222G>A NP_001317922.1:n.118+67222G>A
NM_001330994.1:c.118+67222G>A NP_001317923.1:n.118+67222G>A
XM_005260944.3:c.118+67222G>A XP_005261001.1:n.118+67222G>A
XR_001754829.2:n.288+67222G>A
NM_000830.5:c.118+67222G>A NP_000821.1:n.118+67222G>A
NM_001320616.2:c.118+67222G>A NP_001307545.1:n.118+67222G>A
NM_001320618.2:c.118+67222G>A NP_001307547.1:n.118+67222G>A
NM_001320621.2:c.118+67222G>A NP_001307550.1:n.118+67222G>A
NM_001330993.2:c.118+67222G>A NP_001317922.1:n.118+67222G>A
NM_001330994.2:c.118+67222G>A MANE Select NP_001317923.1:n.118+67222G>A
NM_175611.3:c.118+67222G>A NP_783300.1:n.118+67222G>A
NM_000830.6:c.118+67222G>A NP_000821.1:n.118+67222G>A
NM_001320630.2:c.118+67222G>A NP_001307559.1:n.118+67222G>A
NM_001393424.1:c.118+67222G>A NP_001380353.1:n.118+67222G>A
NM_001393425.1:c.118+67222G>A NP_001380354.1:n.118+67222G>A
NM_001393426.1:c.118+67222G>A NP_001380355.1:n.118+67222G>A