Canonical Allele Identifier: CA1925455294
Gene: GRID1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.86337969A= , CM000672.2:g.86337969A= GRCh38
NC_000010.10:g.88097726A= , CM000672.1:g.88097726A= GRCh37
NC_000010.9:g.88087706A= NCBI36
NG_011875.1:g.33525T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000327946.12:c.235+25972T= MANE Select ENSP00000330148.7:n.235+25972T=
ENST00000327946.11:c.235+25972T= ENSP00000330148.7:n.235+25972T=
ENST00000464741.2:c.235+25972T= ENSP00000433064.1:n.235+25972T=
NM_017551.2:c.235+25972T= NP_060021.1:n.235+25972T=
XM_011539720.1:c.235+25972T= XP_011538022.1:n.235+25972T=
XM_011539720.2:c.235+25972T= XP_011538022.1:n.235+25972T=
NM_017551.3:c.235+25972T= MANE Select NP_060021.1:n.235+25972T=