Canonical Allele Identifier: CA14261453

Gene: GRIN2A

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10021631C>G , CM000678.2:g.10021631C>G	GRCh38
NC_000016.9:g.10115488C>G , CM000678.1:g.10115488C>G	GRCh37
NC_000016.8:g.10022989C>G	NCBI36
NG_011812.1:g.166124G>C
NG_011812.2:g.166124G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.415-83080G>C MANE Select	ENSP00000332549.3:n.415-83080G>C
ENST00000637393.1:c.7-83080G>C	ENSP00000490232.1:n.7-83080G>C
ENST00000674742.1:c.-57-83080G>C	ENSP00000502200.1:n.-57-83080G>C
ENST00000675189.1:n.899-83080G>C
ENST00000675398.1:c.415-83080G>C	ENSP00000502752.1:n.415-83080G>C
ENST00000330684.3:c.415-83080G>C	ENSP00000332549.3:n.415-83080G>C
ENST00000396573.6:c.415-83080G>C	ENSP00000379818.2:n.415-83080G>C
ENST00000562109.5:c.415-83080G>C	ENSP00000454998.1:n.415-83080G>C
ENST00000566670.2:n.256+9694G>C
ENST00000566683.1:n.240+9694G>C
ENST00000568247.3:n.140+5930G>C
NM_000833.4:c.415-83080G>C	NP_000824.1:n.415-83080G>C
NM_001134407.2:c.415-83080G>C	NP_001127879.1:n.415-83080G>C
NM_001134408.2:c.415-83080G>C	NP_001127880.1:n.415-83080G>C
XM_011522456.1:c.255+40520G>C	XP_011520758.1:n.255+40520G>C
XM_011522458.1:c.-58+9694G>C	XP_011520760.1:n.-58+9694G>C
XM_011522459.1:c.-202+9694G>C	XP_011520761.1:n.-202+9694G>C
XM_011522460.1:c.-198+9694G>C	XP_011520762.1:n.-198+9694G>C
XM_011522461.1:c.415-83080G>C	XP_011520763.1:n.415-83080G>C
XM_011522458.3:c.-58+9694G>C	XP_011520760.1:n.-58+9694G>C
XM_011522461.3:c.415-83080G>C	XP_011520763.1:n.415-83080G>C
XM_017023172.1:c.571-83080G>C	XP_016878661.1:n.571-83080G>C
XM_017023173.1:c.571-83080G>C	XP_016878662.1:n.571-83080G>C
NM_001134407.3:c.415-83080G>C MANE Select	NP_001127879.1:n.415-83080G>C
NM_000833.5:c.415-83080G>C	NP_000824.1:n.415-83080G>C