Canonical Allele Identifier: CA477209392

Gene: GRIK4

Linked Data

• gnomAD v4: 11-120956939-T-C
• MyVariant Identifiers: chr11:g.120827648T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.120956939T>C , CM000673.2:g.120956939T>C	GRCh38
NC_000011.9:g.120827648T>C , CM000673.1:g.120827648T>C	GRCh37
NC_000011.8:g.120332858T>C	NCBI36
NG_042194.1:g.450194T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000527524.8:c.1860T>C MANE Select	ENSP00000435648.2:p.Cys620=
ENST00000638419.1:c.1860T>C	ENSP00000492086.1:p.Cys620=
ENST00000438375.2:c.1860T>C	ENSP00000404063.2:p.Cys620=
ENST00000527524.6:c.1860T>C	ENSP00000435648.1:p.Cys620=
ENST00000533291.5:n.2258T>C
NM_001282470.2:c.1860T>C	NP_001269399.1:p.Cys620=
NM_001282473.2:c.1860T>C	NP_001269402.1:p.Cys620=
NM_014619.4:c.1860T>C	NP_055434.2:p.Cys620=
NR_133004.1:n.82+1019A>G
XM_011542783.1:c.2076T>C	XP_011541085.1:p.Cys692=
XM_011542784.1:c.1698T>C	XP_011541086.1:p.Cys566=
XM_011542785.1:c.2076T>C	XP_011541087.1:p.Cys692=
XM_011542786.1:c.1134T>C	XP_011541088.1:p.Cys378=
XM_011542787.1:c.1098T>C	XP_011541089.1:p.Cys366=
XM_011542788.1:c.1098T>C	XP_011541090.1:p.Cys366=
XR_948104.1:n.104+1019A>G
XM_011542784.2:c.1698T>C	XP_011541086.1:p.Cys566=
XM_011542786.2:c.1134T>C	XP_011541088.1:p.Cys378=
XM_011542787.2:c.1098T>C	XP_011541089.1:p.Cys366=
XM_017017621.2:c.1701-3970T>C	XP_016873110.1:n.1701-3970T>C
XM_017017622.2:c.1656T>C	XP_016873111.1:p.Cys552=
NM_014619.5:c.1860T>C MANE Select	NP_055434.2:p.Cys620=
NM_001282470.3:c.1860T>C	NP_001269399.1:p.Cys620=
NM_001282473.3:c.1860T>C	NP_001269402.1:p.Cys620=