Canonical Allele Identifier: CA14869153
Gene: GRIK1 HGNC NCBI
BACH1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.29543953C>T , CM000683.2:g.29543953C>T GRCh38
NC_000021.8:g.30916274C>T , CM000683.1:g.30916274C>T GRCh37
NC_000021.7:g.29838145C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000327783.9:c.2608-6069G>A (GRIK1) MANE Select ENSP00000327687.4:n.2608-6069G>A
ENST00000327783.8:c.2608-6069G>A (GRIK1) ENSP00000327687.4:n.2608-6069G>A
ENST00000389124.6:c.2608-6175G>A (GRIK1) ENSP00000373776.2:n.2608-6175G>A
ENST00000389125.7:c.2563-6568G>A (GRIK1) ENSP00000373777.3:n.2563-6568G>A
ENST00000399913.5:c.2608-6568G>A (GRIK1) ENSP00000382797.1:n.2608-6568G>A
ENST00000399914.5:c.2563-6069G>A (GRIK1) ENSP00000382798.1:n.2563-6069G>A
ENST00000422809.5:c.473-38359C>T (BACH1)
ENST00000468059.1:c.326-53617C>T (BACH1)
ENST00000535441.5:c.2446-6568G>A (GRIK1) ENSP00000446326.2:n.2446-6568G>A
NM_175611.2:c.2563-6568G>A (GRIK1) NP_783300.1:n.2563-6568G>A
XM_005260942.1:c.2563-6069G>A (GRIK1) XP_005260999.1:n.2563-6069G>A
XM_005260943.1:c.2608-6568G>A (GRIK1) XP_005261000.1:n.2608-6568G>A
XM_006723991.1:c.2608-6069G>A (GRIK1) XP_006724054.1:n.2608-6069G>A
NM_001320616.1:c.2608-6568G>A (GRIK1) NP_001307545.1:n.2608-6568G>A
NM_001320618.1:c.2191-6568G>A (GRIK1) NP_001307547.1:n.2191-6568G>A
NM_001320621.1:c.2137-6568G>A (GRIK1) NP_001307550.1:n.2137-6568G>A
NM_001330993.1:c.2563-6069G>A (GRIK1) NP_001317922.1:n.2563-6069G>A
NM_001330994.1:c.2608-6069G>A (GRIK1) NP_001317923.1:n.2608-6069G>A
XR_001754829.2:n.2659-6069G>A (GRIK1)
NM_001320616.2:c.2608-6568G>A (GRIK1) NP_001307545.1:n.2608-6568G>A
NM_001320618.2:c.2191-6568G>A (GRIK1) NP_001307547.1:n.2191-6568G>A
NM_001320621.2:c.2137-6568G>A (GRIK1) NP_001307550.1:n.2137-6568G>A
NM_001330993.2:c.2563-6069G>A (GRIK1) NP_001317922.1:n.2563-6069G>A
NM_001330994.2:c.2608-6069G>A (GRIK1) MANE Select NP_001317923.1:n.2608-6069G>A
NM_175611.3:c.2563-6568G>A (GRIK1) NP_783300.1:n.2563-6568G>A
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