Canonical Allele Identifier: CA394705275

Gene: GRIN2A

Linked Data

• gnomAD v4: 16-9763239-C-A
• MyVariant Identifiers: chr16:g.9857096C>A (hg19) ; chr16:g.9763239C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9763239C>A , CM000678.2:g.9763239C>A	GRCh38
NC_000016.9:g.9857096C>A , CM000678.1:g.9857096C>A	GRCh37
NC_000016.8:g.9764597C>A	NCBI36
NG_011812.1:g.424516G>T
NG_011812.2:g.424516G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.4305G>T MANE Select	ENSP00000332549.3:p.Lys1435Asn
ENST00000535259.6:c.*116G>T	ENSP00000441572.3:n.*116G>T
ENST00000636273.2:n.3555G>T
ENST00000674742.1:c.3834G>T	ENSP00000502200.1:p.Lys1278Asn
ENST00000675398.1:c.*1675G>T	ENSP00000502752.1:n.*1675G>T
ENST00000330684.3:c.4305G>T	ENSP00000332549.3:p.Lys1435Asn
ENST00000396573.6:c.4305G>T	ENSP00000379818.2:p.Lys1435Asn
ENST00000396575.6:c.3894G>T	ENSP00000379820.3:p.Lys1298Asn
ENST00000461292.3:n.3601G>T
ENST00000535259.5:c.*116G>T	ENSP00000441572.2:n.*116G>T
ENST00000562109.5:c.*116G>T	ENSP00000454998.1:n.*116G>T
NM_000833.4:c.4305G>T	NP_000824.1:p.Lys1435Asn
NM_001134407.2:c.4305G>T	NP_001127879.1:p.Lys1435Asn
NM_001134408.2:c.*116G>T	NP_001127880.1:n.*116G>T
XM_011522456.1:c.4146G>T	XP_011520758.1:p.Lys1382Asn
XM_011522457.1:c.4047G>T	XP_011520759.1:p.Lys1349Asn
XM_011522458.1:c.3834G>T	XP_011520760.1:p.Lys1278Asn
XM_011522459.1:c.3834G>T	XP_011520761.1:p.Lys1278Asn
XM_011522460.1:c.3834G>T	XP_011520762.1:p.Lys1278Asn
XM_011522461.1:c.*116G>T	XP_011520763.1:n.*116G>T
XM_011522458.3:c.3834G>T	XP_011520760.1:p.Lys1278Asn
XM_011522461.3:c.*116G>T	XP_011520763.1:n.*116G>T
XM_017023172.1:c.4461G>T	XP_016878661.1:p.Lys1487Asn
XM_017023173.1:c.*116G>T	XP_016878662.1:n.*116G>T
NM_001134407.3:c.4305G>T MANE Select	NP_001127879.1:p.Lys1435Asn
NM_000833.5:c.4305G>T	NP_000824.1:p.Lys1435Asn