Canonical Allele Identifier: CA394798545

Gene: GRIN2A

Linked Data

• dbSNP Id: rs2141630846
• MyVariant Identifiers: chr16:g.10032057T>A (hg19) ; chr16:g.9938200T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9938200T>A , CM000678.2:g.9938200T>A	GRCh38
NC_000016.9:g.10032057T>A , CM000678.1:g.10032057T>A	GRCh37
NC_000016.8:g.9939558T>A	NCBI36
NG_011812.1:g.249555A>T
NG_011812.2:g.249555A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.766A>T MANE Select	ENSP00000332549.3:p.Ile256Phe
ENST00000535259.6:c.295A>T	ENSP00000441572.3:p.Ile99Phe
ENST00000636273.2:n.359A>T
ENST00000637393.1:c.358A>T	ENSP00000490232.1:p.Ile120Phe
ENST00000674742.1:c.295A>T	ENSP00000502200.1:p.Ile99Phe
ENST00000675189.1:n.1250A>T
ENST00000675398.1:c.766A>T	ENSP00000502752.1:p.Ile256Phe
ENST00000330684.3:c.766A>T	ENSP00000332549.3:p.Ile256Phe
ENST00000396573.6:c.766A>T	ENSP00000379818.2:p.Ile256Phe
ENST00000396575.6:c.355A>T	ENSP00000379820.3:p.Ile119Phe
ENST00000461292.3:n.405A>T
ENST00000535259.5:c.355A>T	ENSP00000441572.2:p.Ile119Phe
ENST00000562109.5:c.766A>T	ENSP00000454998.1:p.Ile256Phe
ENST00000566670.2:n.608A>T
ENST00000566683.1:n.241-47100A>T
ENST00000568247.3:n.658A>T
NM_000833.4:c.766A>T	NP_000824.1:p.Ile256Phe
NM_001134407.2:c.766A>T	NP_001127879.1:p.Ile256Phe
NM_001134408.2:c.766A>T	NP_001127880.1:p.Ile256Phe
XM_011522456.1:c.607A>T	XP_011520758.1:p.Ile203Phe
XM_011522457.1:c.508A>T	XP_011520759.1:p.Ile170Phe
XM_011522458.1:c.295A>T	XP_011520760.1:p.Ile99Phe
XM_011522459.1:c.295A>T	XP_011520761.1:p.Ile99Phe
XM_011522460.1:c.295A>T	XP_011520762.1:p.Ile99Phe
XM_011522461.1:c.766A>T	XP_011520763.1:p.Ile256Phe
XM_011522458.3:c.295A>T	XP_011520760.1:p.Ile99Phe
XM_011522461.3:c.766A>T	XP_011520763.1:p.Ile256Phe
XM_017023172.1:c.922A>T	XP_016878661.1:p.Ile308Phe
XM_017023173.1:c.922A>T	XP_016878662.1:p.Ile308Phe
NM_001134407.3:c.766A>T MANE Select	NP_001127879.1:p.Ile256Phe
NM_000833.5:c.766A>T	NP_000824.1:p.Ile256Phe