Canonical Allele Identifier: CA394707735

Gene: GRIN2A

Linked Data

• dbSNP Id: rs2141132110
• MyVariant Identifiers: chr16:g.9857948G>C (hg19) ; chr16:g.9764091G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9764091G>C , CM000678.2:g.9764091G>C	GRCh38
NC_000016.9:g.9857948G>C , CM000678.1:g.9857948G>C	GRCh37
NC_000016.8:g.9765449G>C	NCBI36
NG_011812.1:g.423664C>G
NG_011812.2:g.423664C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.3453C>G MANE Select	ENSP00000332549.3:p.Tyr1151Ter
ENST00000535259.6:c.2982C>G	ENSP00000441572.3:p.Tyr994Ter
ENST00000636273.2:n.3046C>G
ENST00000674742.1:c.2982C>G	ENSP00000502200.1:p.Tyr994Ter
ENST00000675398.1:c.*823C>G	ENSP00000502752.1:n.*823C>G
ENST00000330684.3:c.3453C>G	ENSP00000332549.3:p.Tyr1151Ter
ENST00000396573.6:c.3453C>G	ENSP00000379818.2:p.Tyr1151Ter
ENST00000396575.6:c.3042C>G	ENSP00000379820.3:p.Tyr1014Ter
ENST00000461292.3:n.3092C>G
ENST00000535259.5:c.3042C>G	ENSP00000441572.2:p.Tyr1014Ter
ENST00000562109.5:c.3453C>G	ENSP00000454998.1:p.Tyr1151Ter
NM_000833.4:c.3453C>G	NP_000824.1:p.Tyr1151Ter
NM_001134407.2:c.3453C>G	NP_001127879.1:p.Tyr1151Ter
NM_001134408.2:c.3453C>G	NP_001127880.1:p.Tyr1151Ter
XM_011522456.1:c.3294C>G	XP_011520758.1:p.Tyr1098Ter
XM_011522457.1:c.3195C>G	XP_011520759.1:p.Tyr1065Ter
XM_011522458.1:c.2982C>G	XP_011520760.1:p.Tyr994Ter
XM_011522459.1:c.2982C>G	XP_011520761.1:p.Tyr994Ter
XM_011522460.1:c.2982C>G	XP_011520762.1:p.Tyr994Ter
XM_011522461.1:c.3453C>G	XP_011520763.1:p.Tyr1151Ter
XM_011522458.3:c.2982C>G	XP_011520760.1:p.Tyr994Ter
XM_011522461.3:c.3453C>G	XP_011520763.1:p.Tyr1151Ter
XM_017023172.1:c.3609C>G	XP_016878661.1:p.Tyr1203Ter
XM_017023173.1:c.3609C>G	XP_016878662.1:p.Tyr1203Ter
NM_001134407.3:c.3453C>G MANE Select	NP_001127879.1:p.Tyr1151Ter
NM_000833.5:c.3453C>G	NP_000824.1:p.Tyr1151Ter