Canonical Allele Identifier: CA16620324
Gene: GRIN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 421444
ClinVar RCV Id: RCV000487147 RCV000688647
dbSNP Id: rs1064795143
MyVariant Identifiers: chr16:g.9892126_9892144del (hg19) chr16:g.9798269_9798287del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.9798269_9798287del , CM000678.2:g.9798269_9798287del GRCh38
NC_000016.9:g.9892126_9892144del , CM000678.1:g.9892126_9892144del GRCh37
NC_000016.8:g.9799627_9799645del NCBI36
NG_011812.1:g.389468_389486del
NG_011812.2:g.389468_389486del

Transcript Alleles

HGVS Amino-acid change
ENST00000330684.4:c.2346_2356+8del
ENST00000535259.6:c.1875_1885+8del
ENST00000636273.2:n.1939_1949+8del
ENST00000674742.1:c.1875_1885+8del
ENST00000675398.1:c.2346_2356+8del
ENST00000330684.3:c.2346_2356+8del
ENST00000396573.6:c.2346_2356+8del
ENST00000396575.6:c.1935_1945+8del
ENST00000461292.3:n.1985_1995+8del
ENST00000535259.5:c.1935_1945+8del
ENST00000562109.5:c.2346_2356+8del
NM_000833.4:c.2346_2356+8del
NM_001134407.2:c.2346_2356+8del
NM_001134408.2:c.2346_2356+8del
XM_011522456.1:c.2187_2197+8del
XM_011522457.1:c.2088_2098+8del
XM_011522458.1:c.1875_1885+8del
XM_011522459.1:c.1875_1885+8del
XM_011522460.1:c.1875_1885+8del
XM_011522461.1:c.2346_2356+8del
XR_933062.1:n.300+3547_300+3565del
XR_933063.1:n.300+3547_300+3565del
XM_011522458.3:c.1875_1885+8del
XM_011522461.3:c.2346_2356+8del
XM_017023172.1:c.2502_2512+8del
XM_017023173.1:c.2502_2512+8del
XR_933062.3:n.3304+3547_3304+3565del
XR_933063.3:n.3304+3547_3304+3565del
NM_001134407.3:c.2346_2356+8del
NM_000833.5:c.2346_2356+8del
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