Canonical Allele Identifier: CA1925455289
Gene: GRID1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.86337964T= , CM000672.2:g.86337964T= GRCh38
NC_000010.10:g.88097721T= , CM000672.1:g.88097721T= GRCh37
NC_000010.9:g.88087701T= NCBI36
NG_011875.1:g.33530A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000327946.12:c.235+25977A= MANE Select ENSP00000330148.7:n.235+25977A=
ENST00000327946.11:c.235+25977A= ENSP00000330148.7:n.235+25977A=
ENST00000464741.2:c.235+25977A= ENSP00000433064.1:n.235+25977A=
NM_017551.2:c.235+25977A= NP_060021.1:n.235+25977A=
XM_011539720.1:c.235+25977A= XP_011538022.1:n.235+25977A=
XM_011539720.2:c.235+25977A= XP_011538022.1:n.235+25977A=
NM_017551.3:c.235+25977A= MANE Select NP_060021.1:n.235+25977A=