Canonical Allele Identifier: CA1925358840
Gene: GRID1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.86124268_86124269delinsGC , CM000672.2:g.86124268_86124269delinsGC GRCh38
NC_000010.10:g.87884025_87884026delinsGC , CM000672.1:g.87884025_87884026delinsGC GRCh37
NC_000010.9:g.87874005_87874006delinsGC NCBI36
NG_011875.1:g.247225_247226delinsGC

Transcript Alleles

HGVS Amino-acid change
ENST00000327946.12:c.726+14550_726+14551delinsGC MANE Select ENSP00000330148.7:n.726+14550_726+14551de...
ENST00000327946.11:c.726+14550_726+14551delinsGC ENSP00000330148.7:n.726+14550_726+14551de...
ENST00000464741.2:c.726+14550_726+14551delinsGC ENSP00000433064.1:n.726+14550_726+14551de...
NM_017551.2:c.726+14550_726+14551delinsGC NP_060021.1:n.726+14550_726+14551delinsGC...
XM_011539720.1:c.726+14550_726+14551delinsGC XP_011538022.1:n.726+14550_726+14551delin...
XM_011539720.2:c.726+14550_726+14551delinsGC XP_011538022.1:n.726+14550_726+14551delin...
NM_017551.3:c.726+14550_726+14551delinsGC MANE Select NP_060021.1:n.726+14550_726+14551delinsGC...
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