Canonical Allele Identifier: CA394715083

Gene: GRIN2A

Linked Data

• MyVariant Identifiers: chr16:g.10273866T>G (hg19) ; chr16:g.10180009T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10180009T>G , CM000678.2:g.10180009T>G	GRCh38
NC_000016.9:g.10273866T>G , CM000678.1:g.10273866T>G	GRCh37
NC_000016.8:g.10181367T>G	NCBI36
NG_011812.1:g.7746A>C
NG_011812.2:g.7746A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.403A>C MANE Select	ENSP00000332549.3:p.Met135Leu
ENST00000637334.1:n.82A>C
ENST00000675189.1:n.887A>C
ENST00000675398.1:c.403A>C	ENSP00000502752.1:p.Met135Leu
ENST00000676032.1:n.836A>C
ENST00000330684.3:c.403A>C	ENSP00000332549.3:p.Met135Leu
ENST00000396573.6:c.403A>C	ENSP00000379818.2:p.Met135Leu
ENST00000562109.5:c.403A>C	ENSP00000454998.1:p.Met135Leu
ENST00000566665.1:n.804A>C
NM_000833.4:c.403A>C	NP_000824.1:p.Met135Leu
NM_001134407.2:c.403A>C	NP_001127879.1:p.Met135Leu
NM_001134408.2:c.403A>C	NP_001127880.1:p.Met135Leu
XM_011522461.1:c.403A>C	XP_011520763.1:p.Met135Leu
XM_011522461.3:c.403A>C	XP_011520763.1:p.Met135Leu
XM_017023172.1:c.559A>C	XP_016878661.1:p.Met187Leu
XM_017023173.1:c.559A>C	XP_016878662.1:p.Met187Leu
NM_001134407.3:c.403A>C MANE Select	NP_001127879.1:p.Met135Leu
NM_000833.5:c.403A>C	NP_000824.1:p.Met135Leu