Canonical Allele Identifier: CA2631681658
Gene: GRIN2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.10180449_10180451dup , CM000678.2:g.10180449_10180451dup GRCh38
NC_000016.9:g.10274306_10274308dup , CM000678.1:g.10274306_10274308dup GRCh37
NC_000016.8:g.10181807_10181809dup NCBI36
NG_011812.1:g.7305_7307dup
NG_011812.2:g.7305_7307dup

Transcript Alleles

HGVS Amino-acid change
ENST00000330684.4:c.-18-21_-18-19dup MANE Select ENSP00000332549.3:n.-18-21_-18-19dup
ENST00000636406.1:c.-18-21_-18-19dup ENSP00000490676.1:n.-18-21_-18-19dup
ENST00000637188.1:c.-18-21_-18-19dup ENSP00000489946.1:n.-18-21_-18-19dup
ENST00000675189.1:n.467-21_467-19dup
ENST00000675398.1:c.-18-21_-18-19dup ENSP00000502752.1:n.-18-21_-18-19dup
ENST00000676032.1:n.416-21_416-19dup
ENST00000330684.3:c.-18-21_-18-19dup ENSP00000332549.3:n.-18-21_-18-19dup
ENST00000396573.6:c.-18-21_-18-19dup ENSP00000379818.2:n.-18-21_-18-19dup
ENST00000562109.5:c.-18-21_-18-19dup ENSP00000454998.1:n.-18-21_-18-19dup
ENST00000566665.1:n.384-21_384-19dup
NM_000833.4:c.-18-21_-18-19dup NP_000824.1:n.-18-21_-18-19dup
NM_001134407.2:c.-18-21_-18-19dup NP_001127879.1:n.-18-21_-18-19dup
NM_001134408.2:c.-18-21_-18-19dup NP_001127880.1:n.-18-21_-18-19dup
XM_011522461.1:c.-18-21_-18-19dup XP_011520763.1:n.-18-21_-18-19dup
XM_011522461.3:c.-18-21_-18-19dup XP_011520763.1:n.-18-21_-18-19dup
XM_017023172.1:c.118_120dup XP_016878661.1:p.Leu40_Ser41insLeu
XM_017023173.1:c.118_120dup XP_016878662.1:p.Leu40_Ser41insLeu
NM_001134407.3:c.-18-21_-18-19dup MANE Select NP_001127879.1:n.-18-21_-18-19dup
NM_000833.5:c.-18-21_-18-19dup NP_000824.1:n.-18-21_-18-19dup