Canonical Allele Identifier: CA493702291

Gene: GRIN2A

Linked Data

• dbSNP Id: rs1157097600
• gnomAD v3: 16-9938342-A-G
• gnomAD v4: 16-9938342-A-G
• MyVariant Identifiers: chr16:g.10032199A>G (hg19) ; chr16:g.9938342A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9938342A>G , CM000678.2:g.9938342A>G	GRCh38
NC_000016.9:g.10032199A>G , CM000678.1:g.10032199A>G	GRCh37
NC_000016.8:g.9939700A>G	NCBI36
NG_011812.1:g.249413T>C
NG_011812.2:g.249413T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000330684.4:c.624T>C MANE Select	ENSP00000332549.3:p.Thr208=
ENST00000535259.6:c.153T>C	ENSP00000441572.3:p.Thr51=
ENST00000636273.2:n.217T>C
ENST00000637393.1:c.216T>C	ENSP00000490232.1:p.Thr72=
ENST00000674742.1:c.153T>C	ENSP00000502200.1:p.Thr51=
ENST00000675189.1:n.1108T>C
ENST00000675398.1:c.624T>C	ENSP00000502752.1:p.Thr208=
ENST00000330684.3:c.624T>C	ENSP00000332549.3:p.Thr208=
ENST00000396573.6:c.624T>C	ENSP00000379818.2:p.Thr208=
ENST00000396575.6:c.213T>C	ENSP00000379820.3:p.Thr71=
ENST00000461292.3:n.263T>C
ENST00000535259.5:c.213T>C	ENSP00000441572.2:p.Thr71=
ENST00000562109.5:c.624T>C	ENSP00000454998.1:p.Thr208=
ENST00000566670.2:n.466T>C
ENST00000566683.1:n.241-47242T>C
ENST00000568247.3:n.516T>C
NM_000833.4:c.624T>C	NP_000824.1:p.Thr208=
NM_001134407.2:c.624T>C	NP_001127879.1:p.Thr208=
NM_001134408.2:c.624T>C	NP_001127880.1:p.Thr208=
XM_011522456.1:c.465T>C	XP_011520758.1:p.Thr155=
XM_011522457.1:c.366T>C	XP_011520759.1:p.Thr122=
XM_011522458.1:c.153T>C	XP_011520760.1:p.Thr51=
XM_011522459.1:c.153T>C	XP_011520761.1:p.Thr51=
XM_011522460.1:c.153T>C	XP_011520762.1:p.Thr51=
XM_011522461.1:c.624T>C	XP_011520763.1:p.Thr208=
XM_011522458.3:c.153T>C	XP_011520760.1:p.Thr51=
XM_011522461.3:c.624T>C	XP_011520763.1:p.Thr208=
XM_017023172.1:c.780T>C	XP_016878661.1:p.Thr260=
XM_017023173.1:c.780T>C	XP_016878662.1:p.Thr260=
NM_001134407.3:c.624T>C MANE Select	NP_001127879.1:p.Thr208=
NM_000833.5:c.624T>C	NP_000824.1:p.Thr208=