Canonical Allele Identifier: CA1925358862
Gene: GRID1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.86124302C= , CM000672.2:g.86124302C= GRCh38
NC_000010.10:g.87884059C= , CM000672.1:g.87884059C= GRCh37
NC_000010.9:g.87874039C= NCBI36
NG_011875.1:g.247192G=

Transcript Alleles

HGVS Amino-acid change
ENST00000327946.12:c.726+14517G= MANE Select ENSP00000330148.7:n.726+14517G=
ENST00000327946.11:c.726+14517G= ENSP00000330148.7:n.726+14517G=
ENST00000464741.2:c.726+14517G= ENSP00000433064.1:n.726+14517G=
NM_017551.2:c.726+14517G= NP_060021.1:n.726+14517G=
XM_011539720.1:c.726+14517G= XP_011538022.1:n.726+14517G=
XM_011539720.2:c.726+14517G= XP_011538022.1:n.726+14517G=
NM_017551.3:c.726+14517G= MANE Select NP_060021.1:n.726+14517G=
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