Canonical Allele Identifier: CA1925294372
Gene: GRID1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.85980901_85980902delinsCA , CM000672.2:g.85980901_85980902delinsCA GRCh38
NC_000010.10:g.87740658_87740659delinsCA , CM000672.1:g.87740658_87740659delinsCA GRCh37
NC_000010.9:g.87730638_87730639delinsCA NCBI36
NG_011875.1:g.390592_390593delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000327946.12:c.727-64663_727-64662delinsTG MANE Select ENSP00000330148.7:n.727-64663_727-64662de...
ENST00000327946.11:c.727-64663_727-64662delinsTG ENSP00000330148.7:n.727-64663_727-64662de...
ENST00000464741.2:c.727-64663_727-64662delinsTG ENSP00000433064.1:n.727-64663_727-64662de...
NM_017551.2:c.727-64663_727-64662delinsTG NP_060021.1:n.727-64663_727-64662delinsTG...
XM_011539720.1:c.727-64663_727-64662delinsTG XP_011538022.1:n.727-64663_727-64662delin...
XM_011539720.2:c.727-64663_727-64662delinsTG XP_011538022.1:n.727-64663_727-64662delin...
NM_017551.3:c.727-64663_727-64662delinsTG MANE Select NP_060021.1:n.727-64663_727-64662delinsTG...
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