Canonical Allele Identifier: CA210601558

Gene: GRID1

Linked Data

• dbSNP Id: rs745370989
• MyVariant Identifiers: chr10:g.87608469T>A (hg19) ; chr10:g.85848712T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.85848712T>A , CM000672.2:g.85848712T>A	GRCh38
NC_000010.10:g.87608469T>A , CM000672.1:g.87608469T>A	GRCh37
NC_000010.9:g.87598449T>A	NCBI36
NG_011875.1:g.522782A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000327946.12:c.1233+5784A>T MANE Select	ENSP00000330148.7:n.1233+5784A>T
ENST00000327946.11:c.1233+5784A>T	ENSP00000330148.7:n.1233+5784A>T
ENST00000464741.2:c.1233+5784A>T	ENSP00000433064.1:n.1233+5784A>T
ENST00000536331.5:c.453+5784A>T	ENSP00000444455.2:n.453+5784A>T
NM_017551.2:c.1233+5784A>T	NP_060021.1:n.1233+5784A>T
XM_011539720.1:c.1233+5784A>T	XP_011538022.1:n.1233+5784A>T
XM_011539720.2:c.1233+5784A>T	XP_011538022.1:n.1233+5784A>T
NM_017551.3:c.1233+5784A>T MANE Select	NP_060021.1:n.1233+5784A>T