Canonical Allele Identifier: CA394706026

Gene: GRIN2A

Linked Data

• dbSNP Id: rs1386324916
• MyVariant Identifiers: chr16:g.9857272A>T (hg19) ; chr16:g.9763415A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9763415A>T , CM000678.2:g.9763415A>T	GRCh38
NC_000016.9:g.9857272A>T , CM000678.1:g.9857272A>T	GRCh37
NC_000016.8:g.9764773A>T	NCBI36
NG_011812.1:g.424340T>A
NG_011812.2:g.424340T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.4129T>A MANE Select	ENSP00000332549.3:p.Leu1377Met
ENST00000535259.6:c.3315T>A	ENSP00000441572.3:p.Ala1105=
ENST00000636273.2:n.3379T>A
ENST00000674742.1:c.3658T>A	ENSP00000502200.1:p.Leu1220Met
ENST00000675398.1:c.*1499T>A	ENSP00000502752.1:n.*1499T>A
ENST00000330684.3:c.4129T>A	ENSP00000332549.3:p.Leu1377Met
ENST00000396573.6:c.4129T>A	ENSP00000379818.2:p.Leu1377Met
ENST00000396575.6:c.3718T>A	ENSP00000379820.3:p.Leu1240Met
ENST00000461292.3:n.3425T>A
ENST00000535259.5:c.3375T>A	ENSP00000441572.2:p.Ala1125=
ENST00000562109.5:c.3786T>A	ENSP00000454998.1:p.Ala1262=
NM_000833.4:c.4129T>A	NP_000824.1:p.Leu1377Met
NM_001134407.2:c.4129T>A	NP_001127879.1:p.Leu1377Met
NM_001134408.2:c.3786T>A	NP_001127880.1:p.Ala1262=
XM_011522456.1:c.3970T>A	XP_011520758.1:p.Leu1324Met
XM_011522457.1:c.3871T>A	XP_011520759.1:p.Leu1291Met
XM_011522458.1:c.3658T>A	XP_011520760.1:p.Leu1220Met
XM_011522459.1:c.3658T>A	XP_011520761.1:p.Leu1220Met
XM_011522460.1:c.3658T>A	XP_011520762.1:p.Leu1220Met
XM_011522461.1:c.3786T>A	XP_011520763.1:p.Ala1262=
XM_011522458.3:c.3658T>A	XP_011520760.1:p.Leu1220Met
XM_011522461.3:c.3786T>A	XP_011520763.1:p.Ala1262=
XM_017023172.1:c.4285T>A	XP_016878661.1:p.Leu1429Met
XM_017023173.1:c.3942T>A	XP_016878662.1:p.Ala1314=
NM_001134407.3:c.4129T>A MANE Select	NP_001127879.1:p.Leu1377Met
NM_000833.5:c.4129T>A	NP_000824.1:p.Leu1377Met