Canonical Allele Identifier: CA2534335919

Gene: GRIN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9976690G>T , CM000678.2:g.9976690G>T	GRCh38
NC_000016.9:g.10070547G>T , CM000678.1:g.10070547G>T	GRCh37
NC_000016.8:g.9978048G>T	NCBI36
NG_011812.1:g.211065C>A
NG_011812.2:g.211065C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000330684.4:c.415-38139C>A MANE Select	ENSP00000332549.3:n.415-38139C>A
ENST00000637393.1:c.7-38139C>A	ENSP00000490232.1:n.7-38139C>A
ENST00000674742.1:c.-57-38139C>A	ENSP00000502200.1:n.-57-38139C>A
ENST00000675189.1:n.899-38139C>A
ENST00000675398.1:c.415-38139C>A	ENSP00000502752.1:n.415-38139C>A
ENST00000330684.3:c.415-38139C>A	ENSP00000332549.3:n.415-38139C>A
ENST00000396573.6:c.415-38139C>A	ENSP00000379818.2:n.415-38139C>A
ENST00000562109.5:c.415-38139C>A	ENSP00000454998.1:n.415-38139C>A
ENST00000566670.2:n.257-38139C>A
ENST00000566683.1:n.240+54635C>A
ENST00000568247.3:n.141-33394C>A
NM_000833.4:c.415-38139C>A	NP_000824.1:n.415-38139C>A
NM_001134407.2:c.415-38139C>A	NP_001127879.1:n.415-38139C>A
NM_001134408.2:c.415-38139C>A	NP_001127880.1:n.415-38139C>A
XM_011522456.1:c.256-38139C>A	XP_011520758.1:n.256-38139C>A
XM_011522458.1:c.-57-38139C>A	XP_011520760.1:n.-57-38139C>A
XM_011522459.1:c.-201-21990C>A	XP_011520761.1:n.-201-21990C>A
XM_011522460.1:c.-197-21994C>A	XP_011520762.1:n.-197-21994C>A
XM_011522461.1:c.415-38139C>A	XP_011520763.1:n.415-38139C>A
XM_011522458.3:c.-57-38139C>A	XP_011520760.1:n.-57-38139C>A
XM_011522461.3:c.415-38139C>A	XP_011520763.1:n.415-38139C>A
XM_017023172.1:c.571-38139C>A	XP_016878661.1:n.571-38139C>A
XM_017023173.1:c.571-38139C>A	XP_016878662.1:n.571-38139C>A
NM_001134407.3:c.415-38139C>A MANE Select	NP_001127879.1:n.415-38139C>A
NM_000833.5:c.415-38139C>A	NP_000824.1:n.415-38139C>A