Canonical Allele Identifier: CA394798151

Gene: GRIN2A

Linked Data

• MyVariant Identifiers: chr16:g.10031873T>A (hg19) ; chr16:g.9938016T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9938016T>A , CM000678.2:g.9938016T>A	GRCh38
NC_000016.9:g.10031873T>A , CM000678.1:g.10031873T>A	GRCh37
NC_000016.8:g.9939374T>A	NCBI36
NG_011812.1:g.249739A>T
NG_011812.2:g.249739A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.950A>T MANE Select	ENSP00000332549.3:p.Lys317Met
ENST00000535259.6:c.479A>T	ENSP00000441572.3:p.Lys160Met
ENST00000636273.2:n.543A>T
ENST00000637393.1:c.542A>T	ENSP00000490232.1:p.Lys181Met
ENST00000674742.1:c.479A>T	ENSP00000502200.1:p.Lys160Met
ENST00000675189.1:n.1434A>T
ENST00000675398.1:c.950A>T	ENSP00000502752.1:p.Lys317Met
ENST00000330684.3:c.950A>T	ENSP00000332549.3:p.Lys317Met
ENST00000396573.6:c.950A>T	ENSP00000379818.2:p.Lys317Met
ENST00000396575.6:c.539A>T	ENSP00000379820.3:p.Lys180Met
ENST00000461292.3:n.589A>T
ENST00000535259.5:c.539A>T	ENSP00000441572.2:p.Lys180Met
ENST00000562109.5:c.950A>T	ENSP00000454998.1:p.Lys317Met
ENST00000566683.1:n.241-46916A>T
ENST00000568247.3:n.842A>T
NM_000833.4:c.950A>T	NP_000824.1:p.Lys317Met
NM_001134407.2:c.950A>T	NP_001127879.1:p.Lys317Met
NM_001134408.2:c.950A>T	NP_001127880.1:p.Lys317Met
XM_011522456.1:c.791A>T	XP_011520758.1:p.Lys264Met
XM_011522457.1:c.692A>T	XP_011520759.1:p.Lys231Met
XM_011522458.1:c.479A>T	XP_011520760.1:p.Lys160Met
XM_011522459.1:c.479A>T	XP_011520761.1:p.Lys160Met
XM_011522460.1:c.479A>T	XP_011520762.1:p.Lys160Met
XM_011522461.1:c.950A>T	XP_011520763.1:p.Lys317Met
XM_011522458.3:c.479A>T	XP_011520760.1:p.Lys160Met
XM_011522461.3:c.950A>T	XP_011520763.1:p.Lys317Met
XM_017023172.1:c.1106A>T	XP_016878661.1:p.Lys369Met
XM_017023173.1:c.1106A>T	XP_016878662.1:p.Lys369Met
NM_001134407.3:c.950A>T MANE Select	NP_001127879.1:p.Lys317Met
NM_000833.5:c.950A>T	NP_000824.1:p.Lys317Met