Canonical Allele Identifier: CA16607098

Gene: GRIN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10182048G>C , CM000678.2:g.10182048G>C	GRCh38
NC_000016.9:g.10275905G>C , CM000678.1:g.10275905G>C	GRCh37
NC_000016.8:g.10183406G>C	NCBI36
NG_011812.1:g.5707C>G
NG_011812.2:g.5707C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001134407.3:c.-190C>G MANE Select	NP_001127879.1:n.-190C>G
ENST00000330684.4:c.-190C>G MANE Select	ENSP00000332549.3:n.-190C>G
NM_000833.4:c.-190C>G	NP_000824.1:n.-190C>G
NM_000833.5:c.-190C>G	NP_000824.1:n.-190C>G
NM_001134407.2:c.-190C>G	NP_001127879.1:n.-190C>G
NM_001134408.2:c.-190C>G	NP_001127880.1:n.-190C>G
ENST00000330684.3:c.-190C>G	ENSP00000332549.3:n.-190C>G
ENST00000396573.6:c.-190C>G	ENSP00000379818.2:n.-190C>G
ENST00000566665.1:n.212C>G
ENST00000675189.1:n.295C>G
ENST00000675398.1:c.-190C>G	ENSP00000502752.1:n.-190C>G
ENST00000676032.1:n.244C>G
XM_011522461.1:c.-190C>G	XP_011520763.1:n.-190C>G
XM_011522461.3:c.-190C>G	XP_011520763.1:n.-190C>G