Canonical Allele Identifier: CA394705415

Gene: GRIN2A

Linked Data

• MyVariant Identifiers: chr16:g.9857121T>G (hg19) ; chr16:g.9763264T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9763264T>G , CM000678.2:g.9763264T>G	GRCh38
NC_000016.9:g.9857121T>G , CM000678.1:g.9857121T>G	GRCh37
NC_000016.8:g.9764622T>G	NCBI36
NG_011812.1:g.424491A>C
NG_011812.2:g.424491A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.4280A>C MANE Select	ENSP00000332549.3:p.His1427Pro
ENST00000535259.6:c.*91A>C	ENSP00000441572.3:n.*91A>C
ENST00000636273.2:n.3530A>C
ENST00000674742.1:c.3809A>C	ENSP00000502200.1:p.His1270Pro
ENST00000675398.1:c.*1650A>C	ENSP00000502752.1:n.*1650A>C
ENST00000330684.3:c.4280A>C	ENSP00000332549.3:p.His1427Pro
ENST00000396573.6:c.4280A>C	ENSP00000379818.2:p.His1427Pro
ENST00000396575.6:c.3869A>C	ENSP00000379820.3:p.His1290Pro
ENST00000461292.3:n.3576A>C
ENST00000535259.5:c.*91A>C	ENSP00000441572.2:n.*91A>C
ENST00000562109.5:c.*91A>C	ENSP00000454998.1:n.*91A>C
NM_000833.4:c.4280A>C	NP_000824.1:p.His1427Pro
NM_001134407.2:c.4280A>C	NP_001127879.1:p.His1427Pro
NM_001134408.2:c.*91A>C	NP_001127880.1:n.*91A>C
XM_011522456.1:c.4121A>C	XP_011520758.1:p.His1374Pro
XM_011522457.1:c.4022A>C	XP_011520759.1:p.His1341Pro
XM_011522458.1:c.3809A>C	XP_011520760.1:p.His1270Pro
XM_011522459.1:c.3809A>C	XP_011520761.1:p.His1270Pro
XM_011522460.1:c.3809A>C	XP_011520762.1:p.His1270Pro
XM_011522461.1:c.*91A>C	XP_011520763.1:n.*91A>C
XM_011522458.3:c.3809A>C	XP_011520760.1:p.His1270Pro
XM_011522461.3:c.*91A>C	XP_011520763.1:n.*91A>C
XM_017023172.1:c.4436A>C	XP_016878661.1:p.His1479Pro
XM_017023173.1:c.*91A>C	XP_016878662.1:n.*91A>C
NM_001134407.3:c.4280A>C MANE Select	NP_001127879.1:p.His1427Pro
NM_000833.5:c.4280A>C	NP_000824.1:p.His1427Pro