Canonical Allele Identifier: CA669397480
Gene: GRID1 HGNC NCBI

Linked Data

dbSNP Id: rs1184059551
MyVariant Identifiers: chr10:g.87608506C>G (hg19) chr10:g.85848749C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.85848749C>G , CM000672.2:g.85848749C>G GRCh38
NC_000010.10:g.87608506C>G , CM000672.1:g.87608506C>G GRCh37
NC_000010.9:g.87598486C>G NCBI36
NG_011875.1:g.522745G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000327946.12:c.1233+5747G>C MANE Select ENSP00000330148.7:n.1233+5747G>C
ENST00000327946.11:c.1233+5747G>C ENSP00000330148.7:n.1233+5747G>C
ENST00000464741.2:c.1233+5747G>C ENSP00000433064.1:n.1233+5747G>C
ENST00000536331.5:c.453+5747G>C ENSP00000444455.2:n.453+5747G>C
NM_017551.2:c.1233+5747G>C NP_060021.1:n.1233+5747G>C
XM_011539720.1:c.1233+5747G>C XP_011538022.1:n.1233+5747G>C
XM_011539720.2:c.1233+5747G>C XP_011538022.1:n.1233+5747G>C
NM_017551.3:c.1233+5747G>C MANE Select NP_060021.1:n.1233+5747G>C
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