Canonical Allele Identifier: CA394715326

Gene: GRIN2A

Linked Data

• MyVariant Identifiers: chr16:g.10273971A>G (hg19) ; chr16:g.10180114A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10180114A>G , CM000678.2:g.10180114A>G	GRCh38
NC_000016.9:g.10273971A>G , CM000678.1:g.10273971A>G	GRCh37
NC_000016.8:g.10181472A>G	NCBI36
NG_011812.1:g.7641T>C
NG_011812.2:g.7641T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.298T>C MANE Select	ENSP00000332549.3:p.Phe100Leu
ENST00000675189.1:n.782T>C
ENST00000675398.1:c.298T>C	ENSP00000502752.1:p.Phe100Leu
ENST00000676032.1:n.731T>C
ENST00000330684.3:c.298T>C	ENSP00000332549.3:p.Phe100Leu
ENST00000396573.6:c.298T>C	ENSP00000379818.2:p.Phe100Leu
ENST00000562109.5:c.298T>C	ENSP00000454998.1:p.Phe100Leu
ENST00000566665.1:n.699T>C
NM_000833.4:c.298T>C	NP_000824.1:p.Phe100Leu
NM_001134407.2:c.298T>C	NP_001127879.1:p.Phe100Leu
NM_001134408.2:c.298T>C	NP_001127880.1:p.Phe100Leu
XM_011522461.1:c.298T>C	XP_011520763.1:p.Phe100Leu
XM_011522461.3:c.298T>C	XP_011520763.1:p.Phe100Leu
XM_017023172.1:c.454T>C	XP_016878661.1:p.Phe152Leu
XM_017023173.1:c.454T>C	XP_016878662.1:p.Phe152Leu
NM_001134407.3:c.298T>C MANE Select	NP_001127879.1:p.Phe100Leu
NM_000833.5:c.298T>C	NP_000824.1:p.Phe100Leu