Canonical Allele Identifier: CA394715281

Gene: GRIN2A

Linked Data

• ClinVar Variation Id: 2021389
• ClinVar RCV Id: RCV002862616
• dbSNP Id: rs1555491453
• COSMIC: COSM3505679
• MyVariant Identifiers: chr16:g.10273953G>A (hg19) ; chr16:g.10180096G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10180096G>A , CM000678.2:g.10180096G>A	GRCh38
NC_000016.9:g.10273953G>A , CM000678.1:g.10273953G>A	GRCh37
NC_000016.8:g.10181454G>A	NCBI36
NG_011812.1:g.7659C>T
NG_011812.2:g.7659C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.316C>T MANE Select	ENSP00000332549.3:p.Gln106Ter
ENST00000675189.1:n.800C>T
ENST00000675398.1:c.316C>T	ENSP00000502752.1:p.Gln106Ter
ENST00000676032.1:n.749C>T
ENST00000330684.3:c.316C>T	ENSP00000332549.3:p.Gln106Ter
ENST00000396573.6:c.316C>T	ENSP00000379818.2:p.Gln106Ter
ENST00000562109.5:c.316C>T	ENSP00000454998.1:p.Gln106Ter
ENST00000566665.1:n.717C>T
NM_000833.4:c.316C>T	NP_000824.1:p.Gln106Ter
NM_001134407.2:c.316C>T	NP_001127879.1:p.Gln106Ter
NM_001134408.2:c.316C>T	NP_001127880.1:p.Gln106Ter
XM_011522461.1:c.316C>T	XP_011520763.1:p.Gln106Ter
XM_011522461.3:c.316C>T	XP_011520763.1:p.Gln106Ter
XM_017023172.1:c.472C>T	XP_016878661.1:p.Gln158Ter
XM_017023173.1:c.472C>T	XP_016878662.1:p.Gln158Ter
NM_001134407.3:c.316C>T MANE Select	NP_001127879.1:p.Gln106Ter
NM_000833.5:c.316C>T	NP_000824.1:p.Gln106Ter