Canonical Allele Identifier: CA394709443

Gene: GRIN2A

Linked Data

• dbSNP Id: rs2141137419
• gnomAD v4: 16-9764798-C-G
• MyVariant Identifiers: chr16:g.9858655C>G (hg19) ; chr16:g.9764798C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9764798C>G , CM000678.2:g.9764798C>G	GRCh38
NC_000016.9:g.9858655C>G , CM000678.1:g.9858655C>G	GRCh37
NC_000016.8:g.9766156C>G	NCBI36
NG_011812.1:g.422957G>C
NG_011812.2:g.422957G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.2746G>C MANE Select	ENSP00000332549.3:p.Asp916His
ENST00000535259.6:c.2275G>C	ENSP00000441572.3:p.Asp759His
ENST00000636273.2:n.2339G>C
ENST00000674742.1:c.2275G>C	ENSP00000502200.1:p.Asp759His
ENST00000675398.1:c.*116G>C	ENSP00000502752.1:n.*116G>C
ENST00000330684.3:c.2746G>C	ENSP00000332549.3:p.Asp916His
ENST00000396573.6:c.2746G>C	ENSP00000379818.2:p.Asp916His
ENST00000396575.6:c.2335G>C	ENSP00000379820.3:p.Asp779His
ENST00000461292.3:n.2385G>C
ENST00000535259.5:c.2335G>C	ENSP00000441572.2:p.Asp779His
ENST00000562109.5:c.2746G>C	ENSP00000454998.1:p.Asp916His
NM_000833.4:c.2746G>C	NP_000824.1:p.Asp916His
NM_001134407.2:c.2746G>C	NP_001127879.1:p.Asp916His
NM_001134408.2:c.2746G>C	NP_001127880.1:p.Asp916His
XM_011522456.1:c.2587G>C	XP_011520758.1:p.Asp863His
XM_011522457.1:c.2488G>C	XP_011520759.1:p.Asp830His
XM_011522458.1:c.2275G>C	XP_011520760.1:p.Asp759His
XM_011522459.1:c.2275G>C	XP_011520761.1:p.Asp759His
XM_011522460.1:c.2275G>C	XP_011520762.1:p.Asp759His
XM_011522461.1:c.2746G>C	XP_011520763.1:p.Asp916His
XM_011522458.3:c.2275G>C	XP_011520760.1:p.Asp759His
XM_011522461.3:c.2746G>C	XP_011520763.1:p.Asp916His
XM_017023172.1:c.2902G>C	XP_016878661.1:p.Asp968His
XM_017023173.1:c.2902G>C	XP_016878662.1:p.Asp968His
NM_001134407.3:c.2746G>C MANE Select	NP_001127879.1:p.Asp916His
NM_000833.5:c.2746G>C	NP_000824.1:p.Asp916His