Canonical Allele Identifier: CA493692855

Gene: GRIN2A

Linked Data

• MyVariant Identifiers: chr16:g.9857966C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9764109C>G , CM000678.2:g.9764109C>G	GRCh38
NC_000016.9:g.9857966C>G , CM000678.1:g.9857966C>G	GRCh37
NC_000016.8:g.9765467C>G	NCBI36
NG_011812.1:g.423646G>C
NG_011812.2:g.423646G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.3435G>C MANE Select	ENSP00000332549.3:p.Val1145=
ENST00000535259.6:c.2964G>C	ENSP00000441572.3:p.Val988=
ENST00000636273.2:n.3028G>C
ENST00000674742.1:c.2964G>C	ENSP00000502200.1:p.Val988=
ENST00000675398.1:c.*805G>C	ENSP00000502752.1:n.*805G>C
ENST00000330684.3:c.3435G>C	ENSP00000332549.3:p.Val1145=
ENST00000396573.6:c.3435G>C	ENSP00000379818.2:p.Val1145=
ENST00000396575.6:c.3024G>C	ENSP00000379820.3:p.Val1008=
ENST00000461292.3:n.3074G>C
ENST00000535259.5:c.3024G>C	ENSP00000441572.2:p.Val1008=
ENST00000562109.5:c.3435G>C	ENSP00000454998.1:p.Val1145=
NM_000833.4:c.3435G>C	NP_000824.1:p.Val1145=
NM_001134407.2:c.3435G>C	NP_001127879.1:p.Val1145=
NM_001134408.2:c.3435G>C	NP_001127880.1:p.Val1145=
XM_011522456.1:c.3276G>C	XP_011520758.1:p.Val1092=
XM_011522457.1:c.3177G>C	XP_011520759.1:p.Val1059=
XM_011522458.1:c.2964G>C	XP_011520760.1:p.Val988=
XM_011522459.1:c.2964G>C	XP_011520761.1:p.Val988=
XM_011522460.1:c.2964G>C	XP_011520762.1:p.Val988=
XM_011522461.1:c.3435G>C	XP_011520763.1:p.Val1145=
XM_011522458.3:c.2964G>C	XP_011520760.1:p.Val988=
XM_011522461.3:c.3435G>C	XP_011520763.1:p.Val1145=
XM_017023172.1:c.3591G>C	XP_016878661.1:p.Val1197=
XM_017023173.1:c.3591G>C	XP_016878662.1:p.Val1197=
NM_001134407.3:c.3435G>C MANE Select	NP_001127879.1:p.Val1145=
NM_000833.5:c.3435G>C	NP_000824.1:p.Val1145=