Canonical Allele Identifier: CA394715528

Gene: GRIN2A

Linked Data

• MyVariant Identifiers: chr16:g.10274069A>C (hg19) ; chr16:g.10180212A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10180212A>C , CM000678.2:g.10180212A>C	GRCh38
NC_000016.9:g.10274069A>C , CM000678.1:g.10274069A>C	GRCh37
NC_000016.8:g.10181570A>C	NCBI36
NG_011812.1:g.7543T>G
NG_011812.2:g.7543T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000330684.4:c.200T>G MANE Select	ENSP00000332549.3:p.Val67Gly
ENST00000675189.1:n.684T>G
ENST00000675398.1:c.200T>G	ENSP00000502752.1:p.Val67Gly
ENST00000676032.1:n.633T>G
ENST00000330684.3:c.200T>G	ENSP00000332549.3:p.Val67Gly
ENST00000396573.6:c.200T>G	ENSP00000379818.2:p.Val67Gly
ENST00000562109.5:c.200T>G	ENSP00000454998.1:p.Val67Gly
ENST00000566665.1:n.601T>G
NM_000833.4:c.200T>G	NP_000824.1:p.Val67Gly
NM_001134407.2:c.200T>G	NP_001127879.1:p.Val67Gly
NM_001134408.2:c.200T>G	NP_001127880.1:p.Val67Gly
XM_011522461.1:c.200T>G	XP_011520763.1:p.Val67Gly
XM_011522461.3:c.200T>G	XP_011520763.1:p.Val67Gly
XM_017023172.1:c.356T>G	XP_016878661.1:p.Val119Gly
XM_017023173.1:c.356T>G	XP_016878662.1:p.Val119Gly
NM_001134407.3:c.200T>G MANE Select	NP_001127879.1:p.Val67Gly
NM_000833.5:c.200T>G	NP_000824.1:p.Val67Gly