Canonical Allele Identifier: CA394798221

Gene: GRIN2A

Linked Data

• MyVariant Identifiers: chr16:g.10031904G>C (hg19) ; chr16:g.9938047G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9938047G>C , CM000678.2:g.9938047G>C	GRCh38
NC_000016.9:g.10031904G>C , CM000678.1:g.10031904G>C	GRCh37
NC_000016.8:g.9939405G>C	NCBI36
NG_011812.1:g.249708C>G
NG_011812.2:g.249708C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.919C>G MANE Select	ENSP00000332549.3:p.Leu307Val
ENST00000535259.6:c.448C>G	ENSP00000441572.3:p.Leu150Val
ENST00000636273.2:n.512C>G
ENST00000637393.1:c.511C>G	ENSP00000490232.1:p.Leu171Val
ENST00000674742.1:c.448C>G	ENSP00000502200.1:p.Leu150Val
ENST00000675189.1:n.1403C>G
ENST00000675398.1:c.919C>G	ENSP00000502752.1:p.Leu307Val
ENST00000330684.3:c.919C>G	ENSP00000332549.3:p.Leu307Val
ENST00000396573.6:c.919C>G	ENSP00000379818.2:p.Leu307Val
ENST00000396575.6:c.508C>G	ENSP00000379820.3:p.Leu170Val
ENST00000461292.3:n.558C>G
ENST00000535259.5:c.508C>G	ENSP00000441572.2:p.Leu170Val
ENST00000562109.5:c.919C>G	ENSP00000454998.1:p.Leu307Val
ENST00000566683.1:n.241-46947C>G
ENST00000568247.3:n.811C>G
NM_000833.4:c.919C>G	NP_000824.1:p.Leu307Val
NM_001134407.2:c.919C>G	NP_001127879.1:p.Leu307Val
NM_001134408.2:c.919C>G	NP_001127880.1:p.Leu307Val
XM_011522456.1:c.760C>G	XP_011520758.1:p.Leu254Val
XM_011522457.1:c.661C>G	XP_011520759.1:p.Leu221Val
XM_011522458.1:c.448C>G	XP_011520760.1:p.Leu150Val
XM_011522459.1:c.448C>G	XP_011520761.1:p.Leu150Val
XM_011522460.1:c.448C>G	XP_011520762.1:p.Leu150Val
XM_011522461.1:c.919C>G	XP_011520763.1:p.Leu307Val
XM_011522458.3:c.448C>G	XP_011520760.1:p.Leu150Val
XM_011522461.3:c.919C>G	XP_011520763.1:p.Leu307Val
XM_017023172.1:c.1075C>G	XP_016878661.1:p.Leu359Val
XM_017023173.1:c.1075C>G	XP_016878662.1:p.Leu359Val
NM_001134407.3:c.919C>G MANE Select	NP_001127879.1:p.Leu307Val
NM_000833.5:c.919C>G	NP_000824.1:p.Leu307Val