Canonical Allele Identifier: CA394715062

Gene: GRIN2A

Linked Data

• ClinVar Variation Id: 502679
• ClinVar RCV Id: RCV000597548
• dbSNP Id: rs1555491437
• MyVariant Identifiers: chr16:g.10273863C>A (hg19) ; chr16:g.10180006C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10180006C>A , CM000678.2:g.10180006C>A	GRCh38
NC_000016.9:g.10273863C>A , CM000678.1:g.10273863C>A	GRCh37
NC_000016.8:g.10181364C>A	NCBI36
NG_011812.1:g.7749G>T
NG_011812.2:g.7749G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.406G>T MANE Select	ENSP00000332549.3:p.Ala136Ser
ENST00000637334.1:n.85G>T
ENST00000675189.1:n.890G>T
ENST00000675398.1:c.406G>T	ENSP00000502752.1:p.Ala136Ser
ENST00000676032.1:n.839G>T
ENST00000330684.3:c.406G>T	ENSP00000332549.3:p.Ala136Ser
ENST00000396573.6:c.406G>T	ENSP00000379818.2:p.Ala136Ser
ENST00000562109.5:c.406G>T	ENSP00000454998.1:p.Ala136Ser
ENST00000566665.1:n.807G>T
NM_000833.4:c.406G>T	NP_000824.1:p.Ala136Ser
NM_001134407.2:c.406G>T	NP_001127879.1:p.Ala136Ser
NM_001134408.2:c.406G>T	NP_001127880.1:p.Ala136Ser
XM_011522461.1:c.406G>T	XP_011520763.1:p.Ala136Ser
XM_011522461.3:c.406G>T	XP_011520763.1:p.Ala136Ser
XM_017023172.1:c.562G>T	XP_016878661.1:p.Ala188Ser
XM_017023173.1:c.562G>T	XP_016878662.1:p.Ala188Ser
NM_001134407.3:c.406G>T MANE Select	NP_001127879.1:p.Ala136Ser
NM_000833.5:c.406G>T	NP_000824.1:p.Ala136Ser