Canonical Allele Identifier: CA394715209

Gene: GRIN2A

Linked Data

• ClinVar Variation Id: 1376829
• ClinVar RCV Id: RCV001888187
• dbSNP Id: rs2142388025
• MyVariant Identifiers: chr16:g.10273922A>C (hg19) ; chr16:g.10180065A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10180065A>C , CM000678.2:g.10180065A>C	GRCh38
NC_000016.9:g.10273922A>C , CM000678.1:g.10273922A>C	GRCh37
NC_000016.8:g.10181423A>C	NCBI36
NG_011812.1:g.7690T>G
NG_011812.2:g.7690T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.347T>G MANE Select	ENSP00000332549.3:p.Ile116Ser
ENST00000637334.1:n.26T>G
ENST00000675189.1:n.831T>G
ENST00000675398.1:c.347T>G	ENSP00000502752.1:p.Ile116Ser
ENST00000676032.1:n.780T>G
ENST00000330684.3:c.347T>G	ENSP00000332549.3:p.Ile116Ser
ENST00000396573.6:c.347T>G	ENSP00000379818.2:p.Ile116Ser
ENST00000562109.5:c.347T>G	ENSP00000454998.1:p.Ile116Ser
ENST00000566665.1:n.748T>G
NM_000833.4:c.347T>G	NP_000824.1:p.Ile116Ser
NM_001134407.2:c.347T>G	NP_001127879.1:p.Ile116Ser
NM_001134408.2:c.347T>G	NP_001127880.1:p.Ile116Ser
XM_011522461.1:c.347T>G	XP_011520763.1:p.Ile116Ser
XM_011522461.3:c.347T>G	XP_011520763.1:p.Ile116Ser
XM_017023172.1:c.503T>G	XP_016878661.1:p.Ile168Ser
XM_017023173.1:c.503T>G	XP_016878662.1:p.Ile168Ser
NM_001134407.3:c.347T>G MANE Select	NP_001127879.1:p.Ile116Ser
NM_000833.5:c.347T>G	NP_000824.1:p.Ile116Ser