Canonical Allele Identifier: CA1925386306
Gene: GRID1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.86184814G= , CM000672.2:g.86184814G= GRCh38
NC_000010.10:g.87944571G= , CM000672.1:g.87944571G= GRCh37
NC_000010.9:g.87934551G= NCBI36
NG_011875.1:g.186680C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000327946.12:c.520+21550C= MANE Select ENSP00000330148.7:n.520+21550C=
ENST00000327946.11:c.520+21550C= ENSP00000330148.7:n.520+21550C=
ENST00000464741.2:c.520+21550C= ENSP00000433064.1:n.520+21550C=
NM_017551.2:c.520+21550C= NP_060021.1:n.520+21550C=
XM_011539720.1:c.520+21550C= XP_011538022.1:n.520+21550C=
XM_011539720.2:c.520+21550C= XP_011538022.1:n.520+21550C=
NM_017551.3:c.520+21550C= MANE Select NP_060021.1:n.520+21550C=