Canonical Allele Identifier: CA1925234088
Gene: GRID1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.85848625G= , CM000672.2:g.85848625G= GRCh38
NC_000010.10:g.87608382G= , CM000672.1:g.87608382G= GRCh37
NC_000010.9:g.87598362G= NCBI36
NG_011875.1:g.522869C=

Transcript Alleles

HGVS Amino-acid change
ENST00000327946.12:c.1233+5871C= MANE Select ENSP00000330148.7:n.1233+5871C=
ENST00000327946.11:c.1233+5871C= ENSP00000330148.7:n.1233+5871C=
ENST00000464741.2:c.1233+5871C= ENSP00000433064.1:n.1233+5871C=
ENST00000536331.5:c.453+5871C= ENSP00000444455.2:n.453+5871C=
NM_017551.2:c.1233+5871C= NP_060021.1:n.1233+5871C=
XM_011539720.1:c.1233+5871C= XP_011538022.1:n.1233+5871C=
XM_011539720.2:c.1233+5871C= XP_011538022.1:n.1233+5871C=
NM_017551.3:c.1233+5871C= MANE Select NP_060021.1:n.1233+5871C=
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