Canonical Allele Identifier: CA2573151543

Gene: GRIN2A

Linked Data

• ClinVar Variation Id: 1405214
• ClinVar RCV Id: RCV001903634
• dbSNP Id: rs2142387204

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10179993C>T , CM000678.2:g.10179993C>T	GRCh38
NC_000016.9:g.10273850C>T , CM000678.1:g.10273850C>T	GRCh37
NC_000016.8:g.10181351C>T	NCBI36
NG_011812.1:g.7762G>A
NG_011812.2:g.7762G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.414+5G>A MANE Select	ENSP00000332549.3:n.414+5G>A
ENST00000637334.1:n.93+5G>A
ENST00000637393.1:c.6+5G>A	ENSP00000490232.1:n.6+5G>A
ENST00000675189.1:n.898+5G>A
ENST00000675398.1:c.414+5G>A	ENSP00000502752.1:n.414+5G>A
ENST00000676032.1:n.852G>A
ENST00000330684.3:c.414+5G>A	ENSP00000332549.3:n.414+5G>A
ENST00000396573.6:c.414+5G>A	ENSP00000379818.2:n.414+5G>A
ENST00000562109.5:c.414+5G>A	ENSP00000454998.1:n.414+5G>A
ENST00000566665.1:n.820G>A
NM_000833.4:c.414+5G>A	NP_000824.1:n.414+5G>A
NM_001134407.2:c.414+5G>A	NP_001127879.1:n.414+5G>A
NM_001134408.2:c.414+5G>A	NP_001127880.1:n.414+5G>A
XM_011522461.1:c.414+5G>A	XP_011520763.1:n.414+5G>A
XM_011522461.3:c.414+5G>A	XP_011520763.1:n.414+5G>A
XM_017023172.1:c.570+5G>A	XP_016878661.1:n.570+5G>A
XM_017023173.1:c.570+5G>A	XP_016878662.1:n.570+5G>A
NM_001134407.3:c.414+5G>A MANE Select	NP_001127879.1:n.414+5G>A
NM_000833.5:c.414+5G>A	NP_000824.1:n.414+5G>A