Canonical Allele Identifier: CA493684511

Gene: GRIN2A

Linked Data

• gnomAD v4: 16-9829573-G-C
• MyVariant Identifiers: chr16:g.9923430G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9829573G>C , CM000678.2:g.9829573G>C	GRCh38
NC_000016.9:g.9923430G>C , CM000678.1:g.9923430G>C	GRCh37
NC_000016.8:g.9830931G>C	NCBI36
NG_011812.1:g.358182C>G
NG_011812.2:g.358182C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.1857C>G MANE Select	ENSP00000332549.3:p.Val619=
ENST00000535259.6:c.1386C>G	ENSP00000441572.3:p.Val462=
ENST00000636273.2:n.1450C>G
ENST00000674742.1:c.1386C>G	ENSP00000502200.1:p.Val462=
ENST00000675398.1:c.1857C>G	ENSP00000502752.1:p.Val619=
ENST00000330684.3:c.1857C>G	ENSP00000332549.3:p.Val619=
ENST00000396573.6:c.1857C>G	ENSP00000379818.2:p.Val619=
ENST00000396575.6:c.1446C>G	ENSP00000379820.3:p.Val482=
ENST00000461292.3:n.1496C>G
ENST00000535259.5:c.1446C>G	ENSP00000441572.2:p.Val482=
ENST00000562109.5:c.1857C>G	ENSP00000454998.1:p.Val619=
NM_000833.4:c.1857C>G	NP_000824.1:p.Val619=
NM_001134407.2:c.1857C>G	NP_001127879.1:p.Val619=
NM_001134408.2:c.1857C>G	NP_001127880.1:p.Val619=
XM_011522456.1:c.1698C>G	XP_011520758.1:p.Val566=
XM_011522457.1:c.1599C>G	XP_011520759.1:p.Val533=
XM_011522458.1:c.1386C>G	XP_011520760.1:p.Val462=
XM_011522459.1:c.1386C>G	XP_011520761.1:p.Val462=
XM_011522460.1:c.1386C>G	XP_011520762.1:p.Val462=
XM_011522461.1:c.1857C>G	XP_011520763.1:p.Val619=
XM_011522458.3:c.1386C>G	XP_011520760.1:p.Val462=
XM_011522461.3:c.1857C>G	XP_011520763.1:p.Val619=
XM_017023172.1:c.2013C>G	XP_016878661.1:p.Val671=
XM_017023173.1:c.2013C>G	XP_016878662.1:p.Val671=
NM_001134407.3:c.1857C>G MANE Select	NP_001127879.1:p.Val619=
NM_000833.5:c.1857C>G	NP_000824.1:p.Val619=