Canonical Allele Identifier: CA725899899
Gene: GRIN2A HGNC NCBI

Linked Data

dbSNP Id: rs1181760674

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.9976702C>A , CM000678.2:g.9976702C>A GRCh38
NC_000016.9:g.10070559C>A , CM000678.1:g.10070559C>A GRCh37
NC_000016.8:g.9978060C>A NCBI36
NG_011812.1:g.211053G>T
NG_011812.2:g.211053G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000330684.4:c.415-38151G>T MANE Select ENSP00000332549.3:n.415-38151G>T
ENST00000637393.1:c.7-38151G>T ENSP00000490232.1:n.7-38151G>T
ENST00000674742.1:c.-57-38151G>T ENSP00000502200.1:n.-57-38151G>T
ENST00000675189.1:n.899-38151G>T
ENST00000675398.1:c.415-38151G>T ENSP00000502752.1:n.415-38151G>T
ENST00000330684.3:c.415-38151G>T ENSP00000332549.3:n.415-38151G>T
ENST00000396573.6:c.415-38151G>T ENSP00000379818.2:n.415-38151G>T
ENST00000562109.5:c.415-38151G>T ENSP00000454998.1:n.415-38151G>T
ENST00000566670.2:n.257-38151G>T
ENST00000566683.1:n.240+54623G>T
ENST00000568247.3:n.141-33406G>T
NM_000833.4:c.415-38151G>T NP_000824.1:n.415-38151G>T
NM_001134407.2:c.415-38151G>T NP_001127879.1:n.415-38151G>T
NM_001134408.2:c.415-38151G>T NP_001127880.1:n.415-38151G>T
XM_011522456.1:c.256-38151G>T XP_011520758.1:n.256-38151G>T
XM_011522458.1:c.-57-38151G>T XP_011520760.1:n.-57-38151G>T
XM_011522459.1:c.-201-22002G>T XP_011520761.1:n.-201-22002G>T
XM_011522460.1:c.-197-22006G>T XP_011520762.1:n.-197-22006G>T
XM_011522461.1:c.415-38151G>T XP_011520763.1:n.415-38151G>T
XM_011522458.3:c.-57-38151G>T XP_011520760.1:n.-57-38151G>T
XM_011522461.3:c.415-38151G>T XP_011520763.1:n.415-38151G>T
XM_017023172.1:c.571-38151G>T XP_016878661.1:n.571-38151G>T
XM_017023173.1:c.571-38151G>T XP_016878662.1:n.571-38151G>T
NM_001134407.3:c.415-38151G>T MANE Select NP_001127879.1:n.415-38151G>T
NM_000833.5:c.415-38151G>T NP_000824.1:n.415-38151G>T