Canonical Allele Identifier: CA2206803416

Gene: GRIN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9976714_9976716delinsTCA , CM000678.2:g.9976714_9976716delinsTCA	GRCh38
NC_000016.9:g.10070571_10070573delinsTCA , CM000678.1:g.10070571_10070573delinsTCA	GRCh37
NC_000016.8:g.9978072_9978074delinsTCA	NCBI36
NG_011812.1:g.211039_211041delinsTGA
NG_011812.2:g.211039_211041delinsTGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000330684.4:c.415-38165_415-38163delinsTGA MANE Select	ENSP00000332549.3:n.415-38165_415-38163de...
ENST00000637393.1:c.7-38165_7-38163delinsTGA	ENSP00000490232.1:n.7-38165_7-38163delins...
ENST00000674742.1:c.-57-38165_-57-38163delinsTGA	ENSP00000502200.1:n.-57-38165_-57-38163de...
ENST00000675189.1:n.899-38165_899-38163delinsTGA
ENST00000675398.1:c.415-38165_415-38163delinsTGA	ENSP00000502752.1:n.415-38165_415-38163de...
ENST00000330684.3:c.415-38165_415-38163delinsTGA	ENSP00000332549.3:n.415-38165_415-38163de...
ENST00000396573.6:c.415-38165_415-38163delinsTGA	ENSP00000379818.2:n.415-38165_415-38163de...
ENST00000562109.5:c.415-38165_415-38163delinsTGA	ENSP00000454998.1:n.415-38165_415-38163de...
ENST00000566670.2:n.257-38165_257-38163delinsTGA
ENST00000566683.1:n.240+54609_240+54611delinsTGA
ENST00000568247.3:n.141-33420_141-33418delinsTGA
NM_000833.4:c.415-38165_415-38163delinsTGA	NP_000824.1:n.415-38165_415-38163delinsTG...
NM_001134407.2:c.415-38165_415-38163delinsTGA	NP_001127879.1:n.415-38165_415-38163delin...
NM_001134408.2:c.415-38165_415-38163delinsTGA	NP_001127880.1:n.415-38165_415-38163delin...
XM_011522456.1:c.256-38165_256-38163delinsTGA	XP_011520758.1:n.256-38165_256-38163delin...
XM_011522458.1:c.-57-38165_-57-38163delinsTGA	XP_011520760.1:n.-57-38165_-57-38163delin...
XM_011522459.1:c.-201-22016_-201-22014delinsTGA	XP_011520761.1:n.-201-22016_-201-22014del...
XM_011522460.1:c.-197-22020_-197-22018delinsTGA	XP_011520762.1:n.-197-22020_-197-22018del...
XM_011522461.1:c.415-38165_415-38163delinsTGA	XP_011520763.1:n.415-38165_415-38163delin...
XM_011522458.3:c.-57-38165_-57-38163delinsTGA	XP_011520760.1:n.-57-38165_-57-38163delin...
XM_011522461.3:c.415-38165_415-38163delinsTGA	XP_011520763.1:n.415-38165_415-38163delin...
XM_017023172.1:c.571-38165_571-38163delinsTGA	XP_016878661.1:n.571-38165_571-38163delin...
XM_017023173.1:c.571-38165_571-38163delinsTGA	XP_016878662.1:n.571-38165_571-38163delin...
NM_001134407.3:c.415-38165_415-38163delinsTGA MANE Select	NP_001127879.1:n.415-38165_415-38163delin...
NM_000833.5:c.415-38165_415-38163delinsTGA	NP_000824.1:n.415-38165_415-38163delinsTG...