Canonical Allele Identifier: CA493553039

Gene: GRIN2A

Linked Data

• dbSNP Id: rs1405215133
• gnomAD v2: 16-10274257-C-A
• gnomAD v4: 16-10180400-C-A
• MyVariant Identifiers: chr16:g.10274257C>A (hg19) ; chr16:g.10180400C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10180400C>A , CM000678.2:g.10180400C>A	GRCh38
NC_000016.9:g.10274257C>A , CM000678.1:g.10274257C>A	GRCh37
NC_000016.8:g.10181758C>A	NCBI36
NG_011812.1:g.7355G>T
NG_011812.2:g.7355G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.12G>T MANE Select	ENSP00000332549.3:p.Val4=
ENST00000636406.1:c.12G>T	ENSP00000490676.1:p.Val4=
ENST00000637188.1:c.12G>T	ENSP00000489946.1:p.Val4=
ENST00000675189.1:n.496G>T
ENST00000675398.1:c.12G>T	ENSP00000502752.1:p.Val4=
ENST00000676032.1:n.445G>T
ENST00000330684.3:c.12G>T	ENSP00000332549.3:p.Val4=
ENST00000396573.6:c.12G>T	ENSP00000379818.2:p.Val4=
ENST00000562109.5:c.12G>T	ENSP00000454998.1:p.Val4=
ENST00000566665.1:n.413G>T
NM_000833.4:c.12G>T	NP_000824.1:p.Val4=
NM_001134407.2:c.12G>T	NP_001127879.1:p.Val4=
NM_001134408.2:c.12G>T	NP_001127880.1:p.Val4=
XM_011522461.1:c.12G>T	XP_011520763.1:p.Val4=
XM_011522461.3:c.12G>T	XP_011520763.1:p.Val4=
XM_017023172.1:c.168G>T	XP_016878661.1:p.Val56=
XM_017023173.1:c.168G>T	XP_016878662.1:p.Val56=
NM_001134407.3:c.12G>T MANE Select	NP_001127879.1:p.Val4=
NM_000833.5:c.12G>T	NP_000824.1:p.Val4=