Canonical Allele Identifier: CA2631681629

Gene: GRIN2A

Linked Data

• gnomAD v4: 16-10180420-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10180420C>T , CM000678.2:g.10180420C>T	GRCh38
NC_000016.9:g.10274277C>T , CM000678.1:g.10274277C>T	GRCh37
NC_000016.8:g.10181778C>T	NCBI36
NG_011812.1:g.7335G>A
NG_011812.2:g.7335G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000330684.4:c.-9G>A MANE Select	ENSP00000332549.3:n.-9G>A
ENST00000636406.1:c.-9G>A	ENSP00000490676.1:n.-9G>A
ENST00000637188.1:c.-9G>A	ENSP00000489946.1:n.-9G>A
ENST00000675189.1:n.476G>A
ENST00000675398.1:c.-9G>A	ENSP00000502752.1:n.-9G>A
ENST00000676032.1:n.425G>A
ENST00000330684.3:c.-9G>A	ENSP00000332549.3:n.-9G>A
ENST00000396573.6:c.-9G>A	ENSP00000379818.2:n.-9G>A
ENST00000562109.5:c.-9G>A	ENSP00000454998.1:n.-9G>A
ENST00000566665.1:n.393G>A
NM_000833.4:c.-9G>A	NP_000824.1:n.-9G>A
NM_001134407.2:c.-9G>A	NP_001127879.1:n.-9G>A
NM_001134408.2:c.-9G>A	NP_001127880.1:n.-9G>A
XM_011522461.1:c.-9G>A	XP_011520763.1:n.-9G>A
XM_011522461.3:c.-9G>A	XP_011520763.1:n.-9G>A
XM_017023172.1:c.148G>A	XP_016878661.1:p.Val50Met
XM_017023173.1:c.148G>A	XP_016878662.1:p.Val50Met
NM_001134407.3:c.-9G>A MANE Select	NP_001127879.1:n.-9G>A
NM_000833.5:c.-9G>A	NP_000824.1:n.-9G>A