Canonical Allele Identifier: CA1925358843
Gene: GRID1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.86124276_86124277delinsGC , CM000672.2:g.86124276_86124277delinsGC GRCh38
NC_000010.10:g.87884033_87884034delinsGC , CM000672.1:g.87884033_87884034delinsGC GRCh37
NC_000010.9:g.87874013_87874014delinsGC NCBI36
NG_011875.1:g.247217_247218delinsGC

Transcript Alleles

HGVS Amino-acid change
ENST00000327946.12:c.726+14542_726+14543delinsGC MANE Select ENSP00000330148.7:n.726+14542_726+14543de...
ENST00000327946.11:c.726+14542_726+14543delinsGC ENSP00000330148.7:n.726+14542_726+14543de...
ENST00000464741.2:c.726+14542_726+14543delinsGC ENSP00000433064.1:n.726+14542_726+14543de...
NM_017551.2:c.726+14542_726+14543delinsGC NP_060021.1:n.726+14542_726+14543delinsGC...
XM_011539720.1:c.726+14542_726+14543delinsGC XP_011538022.1:n.726+14542_726+14543delin...
XM_011539720.2:c.726+14542_726+14543delinsGC XP_011538022.1:n.726+14542_726+14543delin...
NM_017551.3:c.726+14542_726+14543delinsGC MANE Select NP_060021.1:n.726+14542_726+14543delinsGC...
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