Canonical Allele Identifier: CA656758516

Gene: GRIN2A

Linked Data

• COSMIC: COSN15665774

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9763120_9763121insA , CM000678.2:g.9763120_9763121insA	GRCh38
NC_000016.9:g.9856977_9856978insA , CM000678.1:g.9856977_9856978insA	GRCh37
NC_000016.8:g.9764478_9764479insA	NCBI36
NG_011812.1:g.424634_424635insT
NG_011812.2:g.424634_424635insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.*28_*29insT MANE Select	ENSP00000332549.3:n.*28_*29insT
ENST00000535259.6:c.*234_*235insT	ENSP00000441572.3:n.*234_*235insT
ENST00000636273.2:n.3673_3674insT
ENST00000674742.1:c.*28_*29insT	ENSP00000502200.1:n.*28_*29insT
ENST00000675398.1:c.*1793_*1794insT	ENSP00000502752.1:n.*1793_*1794insT
ENST00000330684.3:c.*28_*29insT	ENSP00000332549.3:n.*28_*29insT
ENST00000396573.6:c.*28_*29insT	ENSP00000379818.2:n.*28_*29insT
ENST00000396575.6:c.4012_4013insT	ENSP00000379820.3:n.4012_4013insT
ENST00000461292.3:n.3719_3720insT
ENST00000535259.5:c.*234_*235insT	ENSP00000441572.2:n.*234_*235insT
ENST00000562109.5:c.*234_*235insT	ENSP00000454998.1:n.*234_*235insT
NM_000833.4:c.*28_*29insT	NP_000824.1:n.*28_*29insT
NM_001134407.2:c.*28_*29insT	NP_001127879.1:n.*28_*29insT
NM_001134408.2:c.*234_*235insT	NP_001127880.1:n.*234_*235insT
XM_011522456.1:c.*28_*29insT	XP_011520758.1:n.*28_*29insT
XM_011522457.1:c.*28_*29insT	XP_011520759.1:n.*28_*29insT
XM_011522458.1:c.*28_*29insT	XP_011520760.1:n.*28_*29insT
XM_011522459.1:c.*28_*29insT	XP_011520761.1:n.*28_*29insT
XM_011522460.1:c.*28_*29insT	XP_011520762.1:n.*28_*29insT
XM_011522461.1:c.*234_*235insT	XP_011520763.1:n.*234_*235insT
XM_011522458.3:c.*28_*29insT	XP_011520760.1:n.*28_*29insT
XM_011522461.3:c.*234_*235insT	XP_011520763.1:n.*234_*235insT
XM_017023172.1:c.*28_*29insT	XP_016878661.1:n.*28_*29insT
XM_017023173.1:c.*234_*235insT	XP_016878662.1:n.*234_*235insT
NM_001134407.3:c.*28_*29insT MANE Select	NP_001127879.1:n.*28_*29insT
NM_000833.5:c.*28_*29insT	NP_000824.1:n.*28_*29insT