Canonical Allele Identifier: CA394798820

Gene: GRIN2A

Linked Data

• MyVariant Identifiers: chr16:g.10032182T>C (hg19) ; chr16:g.9938325T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9938325T>C , CM000678.2:g.9938325T>C	GRCh38
NC_000016.9:g.10032182T>C , CM000678.1:g.10032182T>C	GRCh37
NC_000016.8:g.9939683T>C	NCBI36
NG_011812.1:g.249430A>G
NG_011812.2:g.249430A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.641A>G MANE Select	ENSP00000332549.3:p.Lys214Arg
ENST00000535259.6:c.170A>G	ENSP00000441572.3:p.Lys57Arg
ENST00000636273.2:n.234A>G
ENST00000637393.1:c.233A>G	ENSP00000490232.1:p.Lys78Arg
ENST00000674742.1:c.170A>G	ENSP00000502200.1:p.Lys57Arg
ENST00000675189.1:n.1125A>G
ENST00000675398.1:c.641A>G	ENSP00000502752.1:p.Lys214Arg
ENST00000330684.3:c.641A>G	ENSP00000332549.3:p.Lys214Arg
ENST00000396573.6:c.641A>G	ENSP00000379818.2:p.Lys214Arg
ENST00000396575.6:c.230A>G	ENSP00000379820.3:p.Lys77Arg
ENST00000461292.3:n.280A>G
ENST00000535259.5:c.230A>G	ENSP00000441572.2:p.Lys77Arg
ENST00000562109.5:c.641A>G	ENSP00000454998.1:p.Lys214Arg
ENST00000566670.2:n.483A>G
ENST00000566683.1:n.241-47225A>G
ENST00000568247.3:n.533A>G
NM_000833.4:c.641A>G	NP_000824.1:p.Lys214Arg
NM_001134407.2:c.641A>G	NP_001127879.1:p.Lys214Arg
NM_001134408.2:c.641A>G	NP_001127880.1:p.Lys214Arg
XM_011522456.1:c.482A>G	XP_011520758.1:p.Lys161Arg
XM_011522457.1:c.383A>G	XP_011520759.1:p.Lys128Arg
XM_011522458.1:c.170A>G	XP_011520760.1:p.Lys57Arg
XM_011522459.1:c.170A>G	XP_011520761.1:p.Lys57Arg
XM_011522460.1:c.170A>G	XP_011520762.1:p.Lys57Arg
XM_011522461.1:c.641A>G	XP_011520763.1:p.Lys214Arg
XM_011522458.3:c.170A>G	XP_011520760.1:p.Lys57Arg
XM_011522461.3:c.641A>G	XP_011520763.1:p.Lys214Arg
XM_017023172.1:c.797A>G	XP_016878661.1:p.Lys266Arg
XM_017023173.1:c.797A>G	XP_016878662.1:p.Lys266Arg
NM_001134407.3:c.641A>G MANE Select	NP_001127879.1:p.Lys214Arg
NM_000833.5:c.641A>G	NP_000824.1:p.Lys214Arg