Canonical Allele Identifier: CA15629106
Gene: GRID1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.85934535T>C , CM000672.2:g.85934535T>C GRCh38
NC_000010.10:g.87694292T>C , CM000672.1:g.87694292T>C GRCh37
NC_000010.9:g.87684272T>C NCBI36
NG_011875.1:g.436959A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000327946.12:c.727-18296A>G MANE Select ENSP00000330148.7:n.727-18296A>G
ENST00000327946.11:c.727-18296A>G ENSP00000330148.7:n.727-18296A>G
ENST00000464741.2:c.727-18296A>G ENSP00000433064.1:n.727-18296A>G
NM_017551.2:c.727-18296A>G NP_060021.1:n.727-18296A>G
XM_011539720.1:c.727-18296A>G XP_011538022.1:n.727-18296A>G
XM_011539720.2:c.727-18296A>G XP_011538022.1:n.727-18296A>G
NM_017551.3:c.727-18296A>G MANE Select NP_060021.1:n.727-18296A>G