Canonical Allele Identifier: CA1925294418
Gene: GRID1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.85981023T= , CM000672.2:g.85981023T= GRCh38
NC_000010.10:g.87740780T= , CM000672.1:g.87740780T= GRCh37
NC_000010.9:g.87730760T= NCBI36
NG_011875.1:g.390471A=

Transcript Alleles

HGVS Amino-acid change
ENST00000327946.12:c.727-64784A= MANE Select ENSP00000330148.7:n.727-64784A=
ENST00000327946.11:c.727-64784A= ENSP00000330148.7:n.727-64784A=
ENST00000464741.2:c.727-64784A= ENSP00000433064.1:n.727-64784A=
NM_017551.2:c.727-64784A= NP_060021.1:n.727-64784A=
XM_011539720.1:c.727-64784A= XP_011538022.1:n.727-64784A=
XM_011539720.2:c.727-64784A= XP_011538022.1:n.727-64784A=
NM_017551.3:c.727-64784A= MANE Select NP_060021.1:n.727-64784A=