Canonical Allele Identifier: CA2206803383
Gene: GRIN2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.9976651_9976653delinsACT , CM000678.2:g.9976651_9976653delinsACT GRCh38
NC_000016.9:g.10070508_10070510delinsACT , CM000678.1:g.10070508_10070510delinsACT GRCh37
NC_000016.8:g.9978009_9978011delinsACT NCBI36
NG_011812.1:g.211102_211104delinsAGT
NG_011812.2:g.211102_211104delinsAGT

Transcript Alleles

HGVS Amino-acid change
ENST00000330684.4:c.415-38102_415-38100delinsAGT MANE Select ENSP00000332549.3:n.415-38102_415-38100de...
ENST00000637393.1:c.7-38102_7-38100delinsAGT ENSP00000490232.1:n.7-38102_7-38100delins...
ENST00000674742.1:c.-57-38102_-57-38100delinsAGT ENSP00000502200.1:n.-57-38102_-57-38100de...
ENST00000675189.1:n.899-38102_899-38100delinsAGT
ENST00000675398.1:c.415-38102_415-38100delinsAGT ENSP00000502752.1:n.415-38102_415-38100de...
ENST00000330684.3:c.415-38102_415-38100delinsAGT ENSP00000332549.3:n.415-38102_415-38100de...
ENST00000396573.6:c.415-38102_415-38100delinsAGT ENSP00000379818.2:n.415-38102_415-38100de...
ENST00000562109.5:c.415-38102_415-38100delinsAGT ENSP00000454998.1:n.415-38102_415-38100de...
ENST00000566670.2:n.257-38102_257-38100delinsAGT
ENST00000566683.1:n.240+54672_240+54674delinsAGT
ENST00000568247.3:n.141-33357_141-33355delinsAGT
NM_000833.4:c.415-38102_415-38100delinsAGT NP_000824.1:n.415-38102_415-38100delinsAG...
NM_001134407.2:c.415-38102_415-38100delinsAGT NP_001127879.1:n.415-38102_415-38100delin...
NM_001134408.2:c.415-38102_415-38100delinsAGT NP_001127880.1:n.415-38102_415-38100delin...
XM_011522456.1:c.256-38102_256-38100delinsAGT XP_011520758.1:n.256-38102_256-38100delin...
XM_011522458.1:c.-57-38102_-57-38100delinsAGT XP_011520760.1:n.-57-38102_-57-38100delin...
XM_011522459.1:c.-201-21953_-201-21951delinsAGT XP_011520761.1:n.-201-21953_-201-21951del...
XM_011522460.1:c.-197-21957_-197-21955delinsAGT XP_011520762.1:n.-197-21957_-197-21955del...
XM_011522461.1:c.415-38102_415-38100delinsAGT XP_011520763.1:n.415-38102_415-38100delin...
XM_011522458.3:c.-57-38102_-57-38100delinsAGT XP_011520760.1:n.-57-38102_-57-38100delin...
XM_011522461.3:c.415-38102_415-38100delinsAGT XP_011520763.1:n.415-38102_415-38100delin...
XM_017023172.1:c.571-38102_571-38100delinsAGT XP_016878661.1:n.571-38102_571-38100delin...
XM_017023173.1:c.571-38102_571-38100delinsAGT XP_016878662.1:n.571-38102_571-38100delin...
NM_001134407.3:c.415-38102_415-38100delinsAGT MANE Select NP_001127879.1:n.415-38102_415-38100delin...
NM_000833.5:c.415-38102_415-38100delinsAGT NP_000824.1:n.415-38102_415-38100delinsAG...