Canonical Allele Identifier: CA394705864

Gene: GRIN2A

Linked Data

• MyVariant Identifiers: chr16:g.9857214A>C (hg19) ; chr16:g.9763357A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9763357A>C , CM000678.2:g.9763357A>C	GRCh38
NC_000016.9:g.9857214A>C , CM000678.1:g.9857214A>C	GRCh37
NC_000016.8:g.9764715A>C	NCBI36
NG_011812.1:g.424398T>G
NG_011812.2:g.424398T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.4187T>G MANE Select	ENSP00000332549.3:p.Val1396Gly
ENST00000535259.6:c.3373T>G	ENSP00000441572.3:p.Ter1125Gly
ENST00000636273.2:n.3437T>G
ENST00000674742.1:c.3716T>G	ENSP00000502200.1:p.Val1239Gly
ENST00000675398.1:c.*1557T>G	ENSP00000502752.1:n.*1557T>G
ENST00000330684.3:c.4187T>G	ENSP00000332549.3:p.Val1396Gly
ENST00000396573.6:c.4187T>G	ENSP00000379818.2:p.Val1396Gly
ENST00000396575.6:c.3776T>G	ENSP00000379820.3:p.Val1259Gly
ENST00000461292.3:n.3483T>G
ENST00000535259.5:c.3433T>G	ENSP00000441572.2:p.Ter1145Gly
ENST00000562109.5:c.3844T>G	ENSP00000454998.1:p.Ter1282Gly
NM_000833.4:c.4187T>G	NP_000824.1:p.Val1396Gly
NM_001134407.2:c.4187T>G	NP_001127879.1:p.Val1396Gly
NM_001134408.2:c.3844T>G	NP_001127880.1:p.Ter1282Gly
XM_011522456.1:c.4028T>G	XP_011520758.1:p.Val1343Gly
XM_011522457.1:c.3929T>G	XP_011520759.1:p.Val1310Gly
XM_011522458.1:c.3716T>G	XP_011520760.1:p.Val1239Gly
XM_011522459.1:c.3716T>G	XP_011520761.1:p.Val1239Gly
XM_011522460.1:c.3716T>G	XP_011520762.1:p.Val1239Gly
XM_011522461.1:c.3844T>G	XP_011520763.1:p.Ter1282Gly
XM_011522458.3:c.3716T>G	XP_011520760.1:p.Val1239Gly
XM_011522461.3:c.3844T>G	XP_011520763.1:p.Ter1282Gly
XM_017023172.1:c.4343T>G	XP_016878661.1:p.Val1448Gly
XM_017023173.1:c.4000T>G	XP_016878662.1:p.Ter1334Gly
NM_001134407.3:c.4187T>G MANE Select	NP_001127879.1:p.Val1396Gly
NM_000833.5:c.4187T>G	NP_000824.1:p.Val1396Gly