Canonical Allele Identifier: CA2631681668
Gene: GRIN2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.10180456G>A , CM000678.2:g.10180456G>A GRCh38
NC_000016.9:g.10274313G>A , CM000678.1:g.10274313G>A GRCh37
NC_000016.8:g.10181814G>A NCBI36
NG_011812.1:g.7299C>T
NG_011812.2:g.7299C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000330684.4:c.-18-27C>T MANE Select ENSP00000332549.3:n.-18-27C>T
ENST00000636406.1:c.-18-27C>T ENSP00000490676.1:n.-18-27C>T
ENST00000637188.1:c.-18-27C>T ENSP00000489946.1:n.-18-27C>T
ENST00000675189.1:n.467-27C>T
ENST00000675398.1:c.-18-27C>T ENSP00000502752.1:n.-18-27C>T
ENST00000676032.1:n.416-27C>T
ENST00000330684.3:c.-18-27C>T ENSP00000332549.3:n.-18-27C>T
ENST00000396573.6:c.-18-27C>T ENSP00000379818.2:n.-18-27C>T
ENST00000562109.5:c.-18-27C>T ENSP00000454998.1:n.-18-27C>T
ENST00000566665.1:n.384-27C>T
NM_000833.4:c.-18-27C>T NP_000824.1:n.-18-27C>T
NM_001134407.2:c.-18-27C>T NP_001127879.1:n.-18-27C>T
NM_001134408.2:c.-18-27C>T NP_001127880.1:n.-18-27C>T
XM_011522461.1:c.-18-27C>T XP_011520763.1:n.-18-27C>T
XM_011522461.3:c.-18-27C>T XP_011520763.1:n.-18-27C>T
XM_017023172.1:c.112C>T XP_016878661.1:p.Pro38Ser
XM_017023173.1:c.112C>T XP_016878662.1:p.Pro38Ser
NM_001134407.3:c.-18-27C>T MANE Select NP_001127879.1:n.-18-27C>T
NM_000833.5:c.-18-27C>T NP_000824.1:n.-18-27C>T