Canonical Allele Identifier: CA2731813492

Gene: GRIN2A

Linked Data

• dbSNP Id: rs2142391752

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10180423A>T , CM000678.2:g.10180423A>T	GRCh38
NC_000016.9:g.10274280A>T , CM000678.1:g.10274280A>T	GRCh37
NC_000016.8:g.10181781A>T	NCBI36
NG_011812.1:g.7332T>A
NG_011812.2:g.7332T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000330684.4:c.-12T>A MANE Select	ENSP00000332549.3:n.-12T>A
ENST00000636406.1:c.-12T>A	ENSP00000490676.1:n.-12T>A
ENST00000637188.1:c.-12T>A	ENSP00000489946.1:n.-12T>A
ENST00000675189.1:n.473T>A
ENST00000675398.1:c.-12T>A	ENSP00000502752.1:n.-12T>A
ENST00000676032.1:n.422T>A
ENST00000330684.3:c.-12T>A	ENSP00000332549.3:n.-12T>A
ENST00000396573.6:c.-12T>A	ENSP00000379818.2:n.-12T>A
ENST00000562109.5:c.-12T>A	ENSP00000454998.1:n.-12T>A
ENST00000566665.1:n.390T>A
NM_000833.4:c.-12T>A	NP_000824.1:n.-12T>A
NM_001134407.2:c.-12T>A	NP_001127879.1:n.-12T>A
NM_001134408.2:c.-12T>A	NP_001127880.1:n.-12T>A
XM_011522461.1:c.-12T>A	XP_011520763.1:n.-12T>A
XM_011522461.3:c.-12T>A	XP_011520763.1:n.-12T>A
XM_017023172.1:c.145T>A	XP_016878661.1:p.Ser49Thr
XM_017023173.1:c.145T>A	XP_016878662.1:p.Ser49Thr
NM_001134407.3:c.-12T>A MANE Select	NP_001127879.1:n.-12T>A
NM_000833.5:c.-12T>A	NP_000824.1:n.-12T>A