Canonical Allele Identifier: CA2206803408

Gene: GRIN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9976698A= , CM000678.2:g.9976698A=	GRCh38
NC_000016.9:g.10070555A= , CM000678.1:g.10070555A=	GRCh37
NC_000016.8:g.9978056A=	NCBI36
NG_011812.1:g.211057T=
NG_011812.2:g.211057T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000330684.4:c.415-38147T= MANE Select	ENSP00000332549.3:n.415-38147T=
ENST00000637393.1:c.7-38147T=	ENSP00000490232.1:n.7-38147T=
ENST00000674742.1:c.-57-38147T=	ENSP00000502200.1:n.-57-38147T=
ENST00000675189.1:n.899-38147T=
ENST00000675398.1:c.415-38147T=	ENSP00000502752.1:n.415-38147T=
ENST00000330684.3:c.415-38147T=	ENSP00000332549.3:n.415-38147T=
ENST00000396573.6:c.415-38147T=	ENSP00000379818.2:n.415-38147T=
ENST00000562109.5:c.415-38147T=	ENSP00000454998.1:n.415-38147T=
ENST00000566670.2:n.257-38147T=
ENST00000566683.1:n.240+54627T=
ENST00000568247.3:n.141-33402T=
NM_000833.4:c.415-38147T=	NP_000824.1:n.415-38147T=
NM_001134407.2:c.415-38147T=	NP_001127879.1:n.415-38147T=
NM_001134408.2:c.415-38147T=	NP_001127880.1:n.415-38147T=
XM_011522456.1:c.256-38147T=	XP_011520758.1:n.256-38147T=
XM_011522458.1:c.-57-38147T=	XP_011520760.1:n.-57-38147T=
XM_011522459.1:c.-201-21998T=	XP_011520761.1:n.-201-21998T=
XM_011522460.1:c.-197-22002T=	XP_011520762.1:n.-197-22002T=
XM_011522461.1:c.415-38147T=	XP_011520763.1:n.415-38147T=
XM_011522458.3:c.-57-38147T=	XP_011520760.1:n.-57-38147T=
XM_011522461.3:c.415-38147T=	XP_011520763.1:n.415-38147T=
XM_017023172.1:c.571-38147T=	XP_016878661.1:n.571-38147T=
XM_017023173.1:c.571-38147T=	XP_016878662.1:n.571-38147T=
NM_001134407.3:c.415-38147T= MANE Select	NP_001127879.1:n.415-38147T=
NM_000833.5:c.415-38147T=	NP_000824.1:n.415-38147T=