Canonical Allele Identifier: CA394798263

Gene: GRIN2A

Linked Data

• MyVariant Identifiers: chr16:g.10031927A>C (hg19) ; chr16:g.9938070A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9938070A>C , CM000678.2:g.9938070A>C	GRCh38
NC_000016.9:g.10031927A>C , CM000678.1:g.10031927A>C	GRCh37
NC_000016.8:g.9939428A>C	NCBI36
NG_011812.1:g.249685T>G
NG_011812.2:g.249685T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.896T>G MANE Select	ENSP00000332549.3:p.Leu299Arg
ENST00000535259.6:c.425T>G	ENSP00000441572.3:p.Leu142Arg
ENST00000636273.2:n.489T>G
ENST00000637393.1:c.488T>G	ENSP00000490232.1:p.Leu163Arg
ENST00000674742.1:c.425T>G	ENSP00000502200.1:p.Leu142Arg
ENST00000675189.1:n.1380T>G
ENST00000675398.1:c.896T>G	ENSP00000502752.1:p.Leu299Arg
ENST00000330684.3:c.896T>G	ENSP00000332549.3:p.Leu299Arg
ENST00000396573.6:c.896T>G	ENSP00000379818.2:p.Leu299Arg
ENST00000396575.6:c.485T>G	ENSP00000379820.3:p.Leu162Arg
ENST00000461292.3:n.535T>G
ENST00000535259.5:c.485T>G	ENSP00000441572.2:p.Leu162Arg
ENST00000562109.5:c.896T>G	ENSP00000454998.1:p.Leu299Arg
ENST00000566683.1:n.241-46970T>G
ENST00000568247.3:n.788T>G
NM_000833.4:c.896T>G	NP_000824.1:p.Leu299Arg
NM_001134407.2:c.896T>G	NP_001127879.1:p.Leu299Arg
NM_001134408.2:c.896T>G	NP_001127880.1:p.Leu299Arg
XM_011522456.1:c.737T>G	XP_011520758.1:p.Leu246Arg
XM_011522457.1:c.638T>G	XP_011520759.1:p.Leu213Arg
XM_011522458.1:c.425T>G	XP_011520760.1:p.Leu142Arg
XM_011522459.1:c.425T>G	XP_011520761.1:p.Leu142Arg
XM_011522460.1:c.425T>G	XP_011520762.1:p.Leu142Arg
XM_011522461.1:c.896T>G	XP_011520763.1:p.Leu299Arg
XM_011522458.3:c.425T>G	XP_011520760.1:p.Leu142Arg
XM_011522461.3:c.896T>G	XP_011520763.1:p.Leu299Arg
XM_017023172.1:c.1052T>G	XP_016878661.1:p.Leu351Arg
XM_017023173.1:c.1052T>G	XP_016878662.1:p.Leu351Arg
NM_001134407.3:c.896T>G MANE Select	NP_001127879.1:p.Leu299Arg
NM_000833.5:c.896T>G	NP_000824.1:p.Leu299Arg