Canonical Allele Identifier: CA725899904
Gene: GRIN2A HGNC NCBI

Linked Data

dbSNP Id: rs1186172606

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.9976717_9976718del , CM000678.2:g.9976717_9976718del GRCh38
NC_000016.9:g.10070574_10070575del , CM000678.1:g.10070574_10070575del GRCh37
NC_000016.8:g.9978075_9978076del NCBI36
NG_011812.1:g.211039_211040del
NG_011812.2:g.211039_211040del

Transcript Alleles

HGVS Amino-acid change
ENST00000330684.4:c.415-38165_415-38164del MANE Select ENSP00000332549.3:n.415-38165_415-38164de...
ENST00000637393.1:c.7-38165_7-38164del ENSP00000490232.1:n.7-38165_7-38164del
ENST00000674742.1:c.-57-38165_-57-38164del ENSP00000502200.1:n.-57-38165_-57-38164de...
ENST00000675189.1:n.899-38165_899-38164del
ENST00000675398.1:c.415-38165_415-38164del ENSP00000502752.1:n.415-38165_415-38164de...
ENST00000330684.3:c.415-38165_415-38164del ENSP00000332549.3:n.415-38165_415-38164de...
ENST00000396573.6:c.415-38165_415-38164del ENSP00000379818.2:n.415-38165_415-38164de...
ENST00000562109.5:c.415-38165_415-38164del ENSP00000454998.1:n.415-38165_415-38164de...
ENST00000566670.2:n.257-38165_257-38164del
ENST00000566683.1:n.240+54609_240+54610del
ENST00000568247.3:n.141-33420_141-33419del
NM_000833.4:c.415-38165_415-38164del NP_000824.1:n.415-38165_415-38164del
NM_001134407.2:c.415-38165_415-38164del NP_001127879.1:n.415-38165_415-38164del
NM_001134408.2:c.415-38165_415-38164del NP_001127880.1:n.415-38165_415-38164del
XM_011522456.1:c.256-38165_256-38164del XP_011520758.1:n.256-38165_256-38164del
XM_011522458.1:c.-57-38165_-57-38164del XP_011520760.1:n.-57-38165_-57-38164del
XM_011522459.1:c.-201-22016_-201-22015del XP_011520761.1:n.-201-22016_-201-22015del...
XM_011522460.1:c.-197-22020_-197-22019del XP_011520762.1:n.-197-22020_-197-22019del...
XM_011522461.1:c.415-38165_415-38164del XP_011520763.1:n.415-38165_415-38164del
XM_011522458.3:c.-57-38165_-57-38164del XP_011520760.1:n.-57-38165_-57-38164del
XM_011522461.3:c.415-38165_415-38164del XP_011520763.1:n.415-38165_415-38164del
XM_017023172.1:c.571-38165_571-38164del XP_016878661.1:n.571-38165_571-38164del
XM_017023173.1:c.571-38165_571-38164del XP_016878662.1:n.571-38165_571-38164del
NM_001134407.3:c.415-38165_415-38164del MANE Select NP_001127879.1:n.415-38165_415-38164del
NM_000833.5:c.415-38165_415-38164del NP_000824.1:n.415-38165_415-38164del