Canonical Allele Identifier: CA2206782665

Gene: GRIN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9938191_9938203delinsTGGGGACAATCCA , CM000678.2:g.9938191_9938203delinsTGGGGACAATCCA	GRCh38
NC_000016.9:g.10032048_10032060delinsTGGGGACAATCCA , CM000678.1:g.10032048_10032060delinsTGGGGACAATCCA	GRCh37
NC_000016.8:g.9939549_9939561delinsTGGGGACAATCCA	NCBI36
NG_011812.1:g.249552_249564delinsTGGATTGTCCCCA
NG_011812.2:g.249552_249564delinsTGGATTGTCCCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.763_775delinsTGGATTGTCCCCA MANE Select	ENSP00000332549.3:p.Trp255=
ENST00000535259.6:c.292_304delinsTGGATTGTCCCCA	ENSP00000441572.3:p.Trp98=
ENST00000636273.2:n.356_368delinsTGGATTGTCCCCA
ENST00000637393.1:c.355_367delinsTGGATTGTCCCCA	ENSP00000490232.1:p.Trp119=
ENST00000674742.1:c.292_304delinsTGGATTGTCCCCA	ENSP00000502200.1:p.Trp98=
ENST00000675189.1:n.1247_1259delinsTGGATTGTCCCCA
ENST00000675398.1:c.763_775delinsTGGATTGTCCCCA	ENSP00000502752.1:p.Trp255=
ENST00000330684.3:c.763_775delinsTGGATTGTCCCCA	ENSP00000332549.3:p.Trp255=
ENST00000396573.6:c.763_775delinsTGGATTGTCCCCA	ENSP00000379818.2:p.Trp255=
ENST00000396575.6:c.352_364delinsTGGATTGTCCCCA	ENSP00000379820.3:p.Trp118=
ENST00000461292.3:n.402_414delinsTGGATTGTCCCCA
ENST00000535259.5:c.352_364delinsTGGATTGTCCCCA	ENSP00000441572.2:p.Trp118=
ENST00000562109.5:c.763_775delinsTGGATTGTCCCCA	ENSP00000454998.1:p.Trp255=
ENST00000566670.2:n.605_617delinsTGGATTGTCCCCA
ENST00000566683.1:n.241-47103_241-47091delinsTGGATTGTCCCCA
ENST00000568247.3:n.655_667delinsTGGATTGTCCCCA
NM_000833.4:c.763_775delinsTGGATTGTCCCCA	NP_000824.1:p.Trp255=
NM_001134407.2:c.763_775delinsTGGATTGTCCCCA	NP_001127879.1:p.Trp255=
NM_001134408.2:c.763_775delinsTGGATTGTCCCCA	NP_001127880.1:p.Trp255=
XM_011522456.1:c.604_616delinsTGGATTGTCCCCA	XP_011520758.1:p.Trp202=
XM_011522457.1:c.505_517delinsTGGATTGTCCCCA	XP_011520759.1:p.Trp169=
XM_011522458.1:c.292_304delinsTGGATTGTCCCCA	XP_011520760.1:p.Trp98=
XM_011522459.1:c.292_304delinsTGGATTGTCCCCA	XP_011520761.1:p.Trp98=
XM_011522460.1:c.292_304delinsTGGATTGTCCCCA	XP_011520762.1:p.Trp98=
XM_011522461.1:c.763_775delinsTGGATTGTCCCCA	XP_011520763.1:p.Trp255=
XM_011522458.3:c.292_304delinsTGGATTGTCCCCA	XP_011520760.1:p.Trp98=
XM_011522461.3:c.763_775delinsTGGATTGTCCCCA	XP_011520763.1:p.Trp255=
XM_017023172.1:c.919_931delinsTGGATTGTCCCCA	XP_016878661.1:p.Trp307=
XM_017023173.1:c.919_931delinsTGGATTGTCCCCA	XP_016878662.1:p.Trp307=
NM_001134407.3:c.763_775delinsTGGATTGTCCCCA MANE Select	NP_001127879.1:p.Trp255=
NM_000833.5:c.763_775delinsTGGATTGTCCCCA	NP_000824.1:p.Trp255=