Canonical Allele Identifier: CA1925294413
Gene: GRID1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.85981010_85981014delinsAGCTT , CM000672.2:g.85981010_85981014delinsAGCTT GRCh38
NC_000010.10:g.87740767_87740771delinsAGCTT , CM000672.1:g.87740767_87740771delinsAGCTT GRCh37
NC_000010.9:g.87730747_87730751delinsAGCTT NCBI36
NG_011875.1:g.390480_390484delinsAAGCT

Transcript Alleles

HGVS Amino-acid change
ENST00000327946.12:c.727-64775_727-64771delinsAAGCT MANE Select ENSP00000330148.7:n.727-64775_727-64771de...
ENST00000327946.11:c.727-64775_727-64771delinsAAGCT ENSP00000330148.7:n.727-64775_727-64771de...
ENST00000464741.2:c.727-64775_727-64771delinsAAGCT ENSP00000433064.1:n.727-64775_727-64771de...
NM_017551.2:c.727-64775_727-64771delinsAAGCT NP_060021.1:n.727-64775_727-64771delinsAA...
XM_011539720.1:c.727-64775_727-64771delinsAAGCT XP_011538022.1:n.727-64775_727-64771delin...
XM_011539720.2:c.727-64775_727-64771delinsAAGCT XP_011538022.1:n.727-64775_727-64771delin...
NM_017551.3:c.727-64775_727-64771delinsAAGCT MANE Select NP_060021.1:n.727-64775_727-64771delinsAA...
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