Canonical Allele Identifier: CA1925234124
Gene: GRID1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.85848678T= , CM000672.2:g.85848678T= GRCh38
NC_000010.10:g.87608435T= , CM000672.1:g.87608435T= GRCh37
NC_000010.9:g.87598415T= NCBI36
NG_011875.1:g.522816A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000327946.12:c.1233+5818A= MANE Select ENSP00000330148.7:n.1233+5818A=
ENST00000327946.11:c.1233+5818A= ENSP00000330148.7:n.1233+5818A=
ENST00000464741.2:c.1233+5818A= ENSP00000433064.1:n.1233+5818A=
ENST00000536331.5:c.453+5818A= ENSP00000444455.2:n.453+5818A=
NM_017551.2:c.1233+5818A= NP_060021.1:n.1233+5818A=
XM_011539720.1:c.1233+5818A= XP_011538022.1:n.1233+5818A=
XM_011539720.2:c.1233+5818A= XP_011538022.1:n.1233+5818A=
NM_017551.3:c.1233+5818A= MANE Select NP_060021.1:n.1233+5818A=
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