Canonical Allele Identifier: CA748485678

Gene: GRIK1

Linked Data

• dbSNP Id: rs455804
• MyVariant Identifiers: chr21:g.31146169A>G (hg19) ; chr21:g.29773850A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.29773850A>G , CM000683.2:g.29773850A>G	GRCh38
NC_000021.8:g.31146169A>G , CM000683.1:g.31146169A>G	GRCh37
NC_000021.7:g.30068040A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000399907.6:c.119-79787T>C	ENSP00000382791.1:n.119-79787T>C
ENST00000327783.9:c.119-79787T>C MANE Select	ENSP00000327687.4:n.119-79787T>C
ENST00000327783.8:c.119-79787T>C	ENSP00000327687.4:n.119-79787T>C
ENST00000389124.6:c.119-79787T>C	ENSP00000373776.2:n.119-79787T>C
ENST00000389125.7:c.119-79787T>C	ENSP00000373777.3:n.119-79787T>C
ENST00000399907.5:c.119-79787T>C	ENSP00000382791.1:n.119-79787T>C
ENST00000399909.5:c.119-79787T>C	ENSP00000382793.1:n.119-79787T>C
ENST00000399913.5:c.119-79787T>C	ENSP00000382797.1:n.119-79787T>C
ENST00000399914.5:c.119-79787T>C	ENSP00000382798.1:n.119-79787T>C
ENST00000472429.1:n.652-79787T>C
NM_000830.3:c.119-79787T>C	NP_000821.1:n.119-79787T>C
NM_175611.2:c.119-79787T>C	NP_783300.1:n.119-79787T>C
XM_005260942.1:c.119-79787T>C	XP_005260999.1:n.119-79787T>C
XM_005260943.1:c.119-79787T>C	XP_005261000.1:n.119-79787T>C
XM_005260944.2:c.119-79787T>C	XP_005261001.1:n.119-79787T>C
XM_006723991.1:c.119-79787T>C	XP_006724054.1:n.119-79787T>C
XM_011529527.1:c.119-79787T>C	XP_011527829.1:n.119-79787T>C
XM_011529528.1:c.119-79787T>C	XP_011527830.1:n.119-79787T>C
NM_000830.4:c.119-79787T>C	NP_000821.1:n.119-79787T>C
NM_001320616.1:c.119-79787T>C	NP_001307545.1:n.119-79787T>C
NM_001320618.1:c.119-83865T>C	NP_001307547.1:n.119-83865T>C
NM_001320621.1:c.119-100686T>C	NP_001307550.1:n.119-100686T>C
NM_001320630.1:c.119-79787T>C	NP_001307559.1:n.119-79787T>C
NM_001330993.1:c.119-79787T>C	NP_001317922.1:n.119-79787T>C
NM_001330994.1:c.119-79787T>C	NP_001317923.1:n.119-79787T>C
XM_005260944.3:c.119-79787T>C	XP_005261001.1:n.119-79787T>C
XR_001754829.2:n.289-79787T>C
NM_000830.5:c.119-79787T>C	NP_000821.1:n.119-79787T>C
NM_001320616.2:c.119-79787T>C	NP_001307545.1:n.119-79787T>C
NM_001320618.2:c.119-83865T>C	NP_001307547.1:n.119-83865T>C
NM_001320621.2:c.119-100686T>C	NP_001307550.1:n.119-100686T>C
NM_001330993.2:c.119-79787T>C	NP_001317922.1:n.119-79787T>C
NM_001330994.2:c.119-79787T>C MANE Select	NP_001317923.1:n.119-79787T>C
NM_175611.3:c.119-79787T>C	NP_783300.1:n.119-79787T>C
NM_000830.6:c.119-79787T>C	NP_000821.1:n.119-79787T>C
NM_001320630.2:c.119-79787T>C	NP_001307559.1:n.119-79787T>C
NM_001393424.1:c.119-79787T>C	NP_001380353.1:n.119-79787T>C
NM_001393425.1:c.119-79787T>C	NP_001380354.1:n.119-79787T>C
NM_001393426.1:c.119-83865T>C	NP_001380355.1:n.119-83865T>C