Canonical Allele Identifier: CA974532298

Gene: GRIN2A

Linked Data

• gnomAD v3: 16-9764207-G-GCC
• gnomAD v4: 16-9764207-G-GCC

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9764207_9764208insCC , CM000678.2:g.9764207_9764208insCC	GRCh38
NC_000016.9:g.9858064_9858065insCC , CM000678.1:g.9858064_9858065insCC	GRCh37
NC_000016.8:g.9765565_9765566insCC	NCBI36
NG_011812.1:g.423547_423548insGG
NG_011812.2:g.423547_423548insGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000330684.4:c.3336_3337insGG MANE Select	ENSP00000332549.3:p.Pro1113GlyfsTer9
ENST00000535259.6:c.2865_2866insGG	ENSP00000441572.3:p.Pro956GlyfsTer9
ENST00000636273.2:n.2929_2930insGG
ENST00000674742.1:c.2865_2866insGG	ENSP00000502200.1:p.Pro956GlyfsTer9
ENST00000675398.1:c.*706_*707insGG	ENSP00000502752.1:n.*706_*707insGG
ENST00000330684.3:c.3336_3337insGG	ENSP00000332549.3:p.Pro1113GlyfsTer9
ENST00000396573.6:c.3336_3337insGG	ENSP00000379818.2:p.Pro1113GlyfsTer9
ENST00000396575.6:c.2925_2926insGG	ENSP00000379820.3:p.Pro976GlyfsTer9
ENST00000461292.3:n.2975_2976insGG
ENST00000535259.5:c.2925_2926insGG	ENSP00000441572.2:p.Pro976GlyfsTer9
ENST00000562109.5:c.3336_3337insGG	ENSP00000454998.1:p.Pro1113GlyfsTer9
NM_000833.4:c.3336_3337insGG	NP_000824.1:p.Pro1113GlyfsTer9
NM_001134407.2:c.3336_3337insGG	NP_001127879.1:p.Pro1113GlyfsTer9
NM_001134408.2:c.3336_3337insGG	NP_001127880.1:p.Pro1113GlyfsTer9
XM_011522456.1:c.3177_3178insGG	XP_011520758.1:p.Pro1060GlyfsTer9
XM_011522457.1:c.3078_3079insGG	XP_011520759.1:p.Pro1027GlyfsTer9
XM_011522458.1:c.2865_2866insGG	XP_011520760.1:p.Pro956GlyfsTer9
XM_011522459.1:c.2865_2866insGG	XP_011520761.1:p.Pro956GlyfsTer9
XM_011522460.1:c.2865_2866insGG	XP_011520762.1:p.Pro956GlyfsTer9
XM_011522461.1:c.3336_3337insGG	XP_011520763.1:p.Pro1113GlyfsTer9
XM_011522458.3:c.2865_2866insGG	XP_011520760.1:p.Pro956GlyfsTer9
XM_011522461.3:c.3336_3337insGG	XP_011520763.1:p.Pro1113GlyfsTer9
XM_017023172.1:c.3492_3493insGG	XP_016878661.1:p.Pro1165GlyfsTer9
XM_017023173.1:c.3492_3493insGG	XP_016878662.1:p.Pro1165GlyfsTer9
NM_001134407.3:c.3336_3337insGG MANE Select	NP_001127879.1:p.Pro1113GlyfsTer9
NM_000833.5:c.3336_3337insGG	NP_000824.1:p.Pro1113GlyfsTer9