Canonical Allele Identifier: CA2741113756
Gene: GRID1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.85980950G>A , CM000672.2:g.85980950G>A GRCh38
NC_000010.10:g.87740707G>A , CM000672.1:g.87740707G>A GRCh37
NC_000010.9:g.87730687G>A NCBI36
NG_011875.1:g.390544C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000327946.12:c.727-64711C>T MANE Select ENSP00000330148.7:n.727-64711C>T
ENST00000327946.11:c.727-64711C>T ENSP00000330148.7:n.727-64711C>T
ENST00000464741.2:c.727-64711C>T ENSP00000433064.1:n.727-64711C>T
NM_017551.2:c.727-64711C>T NP_060021.1:n.727-64711C>T
XM_011539720.1:c.727-64711C>T XP_011538022.1:n.727-64711C>T
XM_011539720.2:c.727-64711C>T XP_011538022.1:n.727-64711C>T
NM_017551.3:c.727-64711C>T MANE Select NP_060021.1:n.727-64711C>T
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