Canonical Allele Identifier: CA394798245

Gene: GRIN2A

Linked Data

• MyVariant Identifiers: chr16:g.10031916C>G (hg19) ; chr16:g.9938059C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9938059C>G , CM000678.2:g.9938059C>G	GRCh38
NC_000016.9:g.10031916C>G , CM000678.1:g.10031916C>G	GRCh37
NC_000016.8:g.9939417C>G	NCBI36
NG_011812.1:g.249696G>C
NG_011812.2:g.249696G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.907G>C MANE Select	ENSP00000332549.3:p.Ala303Pro
ENST00000535259.6:c.436G>C	ENSP00000441572.3:p.Ala146Pro
ENST00000636273.2:n.500G>C
ENST00000637393.1:c.499G>C	ENSP00000490232.1:p.Ala167Pro
ENST00000674742.1:c.436G>C	ENSP00000502200.1:p.Ala146Pro
ENST00000675189.1:n.1391G>C
ENST00000675398.1:c.907G>C	ENSP00000502752.1:p.Ala303Pro
ENST00000330684.3:c.907G>C	ENSP00000332549.3:p.Ala303Pro
ENST00000396573.6:c.907G>C	ENSP00000379818.2:p.Ala303Pro
ENST00000396575.6:c.496G>C	ENSP00000379820.3:p.Ala166Pro
ENST00000461292.3:n.546G>C
ENST00000535259.5:c.496G>C	ENSP00000441572.2:p.Ala166Pro
ENST00000562109.5:c.907G>C	ENSP00000454998.1:p.Ala303Pro
ENST00000566683.1:n.241-46959G>C
ENST00000568247.3:n.799G>C
NM_000833.4:c.907G>C	NP_000824.1:p.Ala303Pro
NM_001134407.2:c.907G>C	NP_001127879.1:p.Ala303Pro
NM_001134408.2:c.907G>C	NP_001127880.1:p.Ala303Pro
XM_011522456.1:c.748G>C	XP_011520758.1:p.Ala250Pro
XM_011522457.1:c.649G>C	XP_011520759.1:p.Ala217Pro
XM_011522458.1:c.436G>C	XP_011520760.1:p.Ala146Pro
XM_011522459.1:c.436G>C	XP_011520761.1:p.Ala146Pro
XM_011522460.1:c.436G>C	XP_011520762.1:p.Ala146Pro
XM_011522461.1:c.907G>C	XP_011520763.1:p.Ala303Pro
XM_011522458.3:c.436G>C	XP_011520760.1:p.Ala146Pro
XM_011522461.3:c.907G>C	XP_011520763.1:p.Ala303Pro
XM_017023172.1:c.1063G>C	XP_016878661.1:p.Ala355Pro
XM_017023173.1:c.1063G>C	XP_016878662.1:p.Ala355Pro
NM_001134407.3:c.907G>C MANE Select	NP_001127879.1:p.Ala303Pro
NM_000833.5:c.907G>C	NP_000824.1:p.Ala303Pro