Canonical Allele Identifier: CA394709067

Gene: GRIN2A

Linked Data

• MyVariant Identifiers: chr16:g.9858483T>C (hg19) ; chr16:g.9764626T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9764626T>C , CM000678.2:g.9764626T>C	GRCh38
NC_000016.9:g.9858483T>C , CM000678.1:g.9858483T>C	GRCh37
NC_000016.8:g.9765984T>C	NCBI36
NG_011812.1:g.423129A>G
NG_011812.2:g.423129A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.2918A>G MANE Select	ENSP00000332549.3:p.Asp973Gly
ENST00000535259.6:c.2447A>G	ENSP00000441572.3:p.Asp816Gly
ENST00000636273.2:n.2511A>G
ENST00000674742.1:c.2447A>G	ENSP00000502200.1:p.Asp816Gly
ENST00000675398.1:c.*288A>G	ENSP00000502752.1:n.*288A>G
ENST00000330684.3:c.2918A>G	ENSP00000332549.3:p.Asp973Gly
ENST00000396573.6:c.2918A>G	ENSP00000379818.2:p.Asp973Gly
ENST00000396575.6:c.2507A>G	ENSP00000379820.3:p.Asp836Gly
ENST00000461292.3:n.2557A>G
ENST00000535259.5:c.2507A>G	ENSP00000441572.2:p.Asp836Gly
ENST00000562109.5:c.2918A>G	ENSP00000454998.1:p.Asp973Gly
NM_000833.4:c.2918A>G	NP_000824.1:p.Asp973Gly
NM_001134407.2:c.2918A>G	NP_001127879.1:p.Asp973Gly
NM_001134408.2:c.2918A>G	NP_001127880.1:p.Asp973Gly
XM_011522456.1:c.2759A>G	XP_011520758.1:p.Asp920Gly
XM_011522457.1:c.2660A>G	XP_011520759.1:p.Asp887Gly
XM_011522458.1:c.2447A>G	XP_011520760.1:p.Asp816Gly
XM_011522459.1:c.2447A>G	XP_011520761.1:p.Asp816Gly
XM_011522460.1:c.2447A>G	XP_011520762.1:p.Asp816Gly
XM_011522461.1:c.2918A>G	XP_011520763.1:p.Asp973Gly
XM_011522458.3:c.2447A>G	XP_011520760.1:p.Asp816Gly
XM_011522461.3:c.2918A>G	XP_011520763.1:p.Asp973Gly
XM_017023172.1:c.3074A>G	XP_016878661.1:p.Asp1025Gly
XM_017023173.1:c.3074A>G	XP_016878662.1:p.Asp1025Gly
NM_001134407.3:c.2918A>G MANE Select	NP_001127879.1:p.Asp973Gly
NM_000833.5:c.2918A>G	NP_000824.1:p.Asp973Gly