Canonical Allele Identifier: CA493693764

Gene: GRIN2A

Linked Data

• MyVariant Identifiers: chr16:g.10274086C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10180229C>G , CM000678.2:g.10180229C>G	GRCh38
NC_000016.9:g.10274086C>G , CM000678.1:g.10274086C>G	GRCh37
NC_000016.8:g.10181587C>G	NCBI36
NG_011812.1:g.7526G>C
NG_011812.2:g.7526G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000330684.4:c.183G>C MANE Select	ENSP00000332549.3:p.Ala61=
ENST00000675189.1:n.667G>C
ENST00000675398.1:c.183G>C	ENSP00000502752.1:p.Ala61=
ENST00000676032.1:n.616G>C
ENST00000330684.3:c.183G>C	ENSP00000332549.3:p.Ala61=
ENST00000396573.6:c.183G>C	ENSP00000379818.2:p.Ala61=
ENST00000562109.5:c.183G>C	ENSP00000454998.1:p.Ala61=
ENST00000566665.1:n.584G>C
NM_000833.4:c.183G>C	NP_000824.1:p.Ala61=
NM_001134407.2:c.183G>C	NP_001127879.1:p.Ala61=
NM_001134408.2:c.183G>C	NP_001127880.1:p.Ala61=
XM_011522461.1:c.183G>C	XP_011520763.1:p.Ala61=
XM_011522461.3:c.183G>C	XP_011520763.1:p.Ala61=
XM_017023172.1:c.339G>C	XP_016878661.1:p.Ala113=
XM_017023173.1:c.339G>C	XP_016878662.1:p.Ala113=
NM_001134407.3:c.183G>C MANE Select	NP_001127879.1:p.Ala61=
NM_000833.5:c.183G>C	NP_000824.1:p.Ala61=