Canonical Allele Identifier: CA277616130

Gene: GRIN2A

Linked Data

• dbSNP Id: rs760642357
• gnomAD v2: 16-10274272-C-T
• gnomAD v3: 16-10180415-C-T
• gnomAD v4: 16-10180415-C-T
• MyVariant Identifiers: chr16:g.10274272C>T (hg19) ; chr16:g.10180415C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10180415C>T , CM000678.2:g.10180415C>T	GRCh38
NC_000016.9:g.10274272C>T , CM000678.1:g.10274272C>T	GRCh37
NC_000016.8:g.10181773C>T	NCBI36
NG_011812.1:g.7340G>A
NG_011812.2:g.7340G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000330684.4:c.-4G>A MANE Select	ENSP00000332549.3:n.-4G>A
ENST00000636406.1:c.-4G>A	ENSP00000490676.1:n.-4G>A
ENST00000637188.1:c.-4G>A	ENSP00000489946.1:n.-4G>A
ENST00000675189.1:n.481G>A
ENST00000675398.1:c.-4G>A	ENSP00000502752.1:n.-4G>A
ENST00000676032.1:n.430G>A
ENST00000330684.3:c.-4G>A	ENSP00000332549.3:n.-4G>A
ENST00000396573.6:c.-4G>A	ENSP00000379818.2:n.-4G>A
ENST00000562109.5:c.-4G>A	ENSP00000454998.1:n.-4G>A
ENST00000566665.1:n.398G>A
NM_000833.4:c.-4G>A	NP_000824.1:n.-4G>A
NM_001134407.2:c.-4G>A	NP_001127879.1:n.-4G>A
NM_001134408.2:c.-4G>A	NP_001127880.1:n.-4G>A
XM_011522461.1:c.-4G>A	XP_011520763.1:n.-4G>A
XM_011522461.3:c.-4G>A	XP_011520763.1:n.-4G>A
XM_017023172.1:c.153G>A	XP_016878661.1:p.Ala51=
XM_017023173.1:c.153G>A	XP_016878662.1:p.Ala51=
NM_001134407.3:c.-4G>A MANE Select	NP_001127879.1:n.-4G>A
NM_000833.5:c.-4G>A	NP_000824.1:n.-4G>A