Canonical Allele Identifier: CA2570371131
Gene: GRIN2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.9976587_9976588insCACC , CM000678.2:g.9976587_9976588insCACC GRCh38
NC_000016.9:g.10070444_10070445insCACC , CM000678.1:g.10070444_10070445insCACC GRCh37
NC_000016.8:g.9977945_9977946insCACC NCBI36
NG_011812.1:g.211167_211168insGGTG
NG_011812.2:g.211167_211168insGGTG

Transcript Alleles

HGVS Amino-acid change
ENST00000330684.4:c.415-38037_415-38036insGGTG MANE Select ENSP00000332549.3:n.415-38037_415-38036in...
ENST00000637393.1:c.7-38037_7-38036insGGTG ENSP00000490232.1:n.7-38037_7-38036insGGT...
ENST00000674742.1:c.-57-38037_-57-38036insGGTG ENSP00000502200.1:n.-57-38037_-57-38036in...
ENST00000675189.1:n.899-38037_899-38036insGGTG
ENST00000675398.1:c.415-38037_415-38036insGGTG ENSP00000502752.1:n.415-38037_415-38036in...
ENST00000330684.3:c.415-38037_415-38036insGGTG ENSP00000332549.3:n.415-38037_415-38036in...
ENST00000396573.6:c.415-38037_415-38036insGGTG ENSP00000379818.2:n.415-38037_415-38036in...
ENST00000562109.5:c.415-38037_415-38036insGGTG ENSP00000454998.1:n.415-38037_415-38036in...
ENST00000566670.2:n.257-38037_257-38036insGGTG
ENST00000566683.1:n.240+54737_240+54738insGGTG
ENST00000568247.3:n.141-33292_141-33291insGGTG
NM_000833.4:c.415-38037_415-38036insGGTG NP_000824.1:n.415-38037_415-38036insGGTG
NM_001134407.2:c.415-38037_415-38036insGGTG NP_001127879.1:n.415-38037_415-38036insGG...
NM_001134408.2:c.415-38037_415-38036insGGTG NP_001127880.1:n.415-38037_415-38036insGG...
XM_011522456.1:c.256-38037_256-38036insGGTG XP_011520758.1:n.256-38037_256-38036insGG...
XM_011522458.1:c.-57-38037_-57-38036insGGTG XP_011520760.1:n.-57-38037_-57-38036insGG...
XM_011522459.1:c.-201-21888_-201-21887insGGTG XP_011520761.1:n.-201-21888_-201-21887ins...
XM_011522460.1:c.-197-21892_-197-21891insGGTG XP_011520762.1:n.-197-21892_-197-21891ins...
XM_011522461.1:c.415-38037_415-38036insGGTG XP_011520763.1:n.415-38037_415-38036insGG...
XM_011522458.3:c.-57-38037_-57-38036insGGTG XP_011520760.1:n.-57-38037_-57-38036insGG...
XM_011522461.3:c.415-38037_415-38036insGGTG XP_011520763.1:n.415-38037_415-38036insGG...
XM_017023172.1:c.571-38037_571-38036insGGTG XP_016878661.1:n.571-38037_571-38036insGG...
XM_017023173.1:c.571-38037_571-38036insGGTG XP_016878662.1:n.571-38037_571-38036insGG...
NM_001134407.3:c.415-38037_415-38036insGGTG MANE Select NP_001127879.1:n.415-38037_415-38036insGG...
NM_000833.5:c.415-38037_415-38036insGGTG NP_000824.1:n.415-38037_415-38036insGGTG