Canonical Allele Identifier: CA2206912920

Gene: GRIN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10180330_10180345delinsCCGCCGCCGCGCTCGG , CM000678.2:g.10180330_10180345delinsCCGCCGCCGCGCTCGG	GRCh38
NC_000016.9:g.10274187_10274202delinsCCGCCGCCGCGCTCGG , CM000678.1:g.10274187_10274202delinsCCGCCGCCGCGCTCGG	GRCh37
NC_000016.8:g.10181688_10181703delinsCCGCCGCCGCGCTCGG	NCBI36
NG_011812.1:g.7410_7425delinsCCGAGCGCGGCGGCGG
NG_011812.2:g.7410_7425delinsCCGAGCGCGGCGGCGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000330684.4:c.67_82delinsCCGAGCGCGGCGGCGG MANE Select	ENSP00000332549.3:p.Pro23=
ENST00000675189.1:n.551_566delinsCCGAGCGCGGCGGCGG
ENST00000675398.1:c.67_82delinsCCGAGCGCGGCGGCGG	ENSP00000502752.1:p.Pro23=
ENST00000676032.1:n.500_515delinsCCGAGCGCGGCGGCGG
ENST00000330684.3:c.67_82delinsCCGAGCGCGGCGGCGG	ENSP00000332549.3:p.Pro23=
ENST00000396573.6:c.67_82delinsCCGAGCGCGGCGGCGG	ENSP00000379818.2:p.Pro23=
ENST00000562109.5:c.67_82delinsCCGAGCGCGGCGGCGG	ENSP00000454998.1:p.Pro23=
ENST00000566665.1:n.468_483delinsCCGAGCGCGGCGGCGG
NM_000833.4:c.67_82delinsCCGAGCGCGGCGGCGG	NP_000824.1:p.Pro23=
NM_001134407.2:c.67_82delinsCCGAGCGCGGCGGCGG	NP_001127879.1:p.Pro23=
NM_001134408.2:c.67_82delinsCCGAGCGCGGCGGCGG	NP_001127880.1:p.Pro23=
XM_011522461.1:c.67_82delinsCCGAGCGCGGCGGCGG	XP_011520763.1:p.Pro23=
XM_011522461.3:c.67_82delinsCCGAGCGCGGCGGCGG	XP_011520763.1:p.Pro23=
XM_017023172.1:c.223_238delinsCCGAGCGCGGCGGCGG	XP_016878661.1:p.Pro75=
XM_017023173.1:c.223_238delinsCCGAGCGCGGCGGCGG	XP_016878662.1:p.Pro75=
NM_001134407.3:c.67_82delinsCCGAGCGCGGCGGCGG MANE Select	NP_001127879.1:p.Pro23=
NM_000833.5:c.67_82delinsCCGAGCGCGGCGGCGG	NP_000824.1:p.Pro23=