Canonical Allele Identifier: CA2631681560

Gene: GRIN2A

Linked Data

• gnomAD v4: 16-10179966-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10179966G>C , CM000678.2:g.10179966G>C	GRCh38
NC_000016.9:g.10273823G>C , CM000678.1:g.10273823G>C	GRCh37
NC_000016.8:g.10181324G>C	NCBI36
NG_011812.1:g.7789C>G
NG_011812.2:g.7789C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.414+32C>G MANE Select	ENSP00000332549.3:n.414+32C>G
ENST00000637334.1:n.93+32C>G
ENST00000637393.1:c.6+32C>G	ENSP00000490232.1:n.6+32C>G
ENST00000675189.1:n.898+32C>G
ENST00000675398.1:c.414+32C>G	ENSP00000502752.1:n.414+32C>G
ENST00000676032.1:n.879C>G
ENST00000330684.3:c.414+32C>G	ENSP00000332549.3:n.414+32C>G
ENST00000396573.6:c.414+32C>G	ENSP00000379818.2:n.414+32C>G
ENST00000562109.5:c.414+32C>G	ENSP00000454998.1:n.414+32C>G
ENST00000566665.1:n.847C>G
NM_000833.4:c.414+32C>G	NP_000824.1:n.414+32C>G
NM_001134407.2:c.414+32C>G	NP_001127879.1:n.414+32C>G
NM_001134408.2:c.414+32C>G	NP_001127880.1:n.414+32C>G
XM_011522461.1:c.414+32C>G	XP_011520763.1:n.414+32C>G
XM_011522461.3:c.414+32C>G	XP_011520763.1:n.414+32C>G
XM_017023172.1:c.570+32C>G	XP_016878661.1:n.570+32C>G
XM_017023173.1:c.570+32C>G	XP_016878662.1:n.570+32C>G
NM_001134407.3:c.414+32C>G MANE Select	NP_001127879.1:n.414+32C>G
NM_000833.5:c.414+32C>G	NP_000824.1:n.414+32C>G