Canonical Allele Identifier: CA1884318137
Gene: GRIN1 HGNC NCBI

Linked Data

dbSNP Id: rs1832029377

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137139125_137139127del , CM000671.2:g.137139125_137139127del GRCh38
NC_000009.11:g.140033577_140033579del , CM000671.1:g.140033577_140033579del GRCh37
NC_000009.10:g.139153398_139153400del NCBI36
NG_011507.1:g.4969_4971del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371560.5:c.-362_-360del ENSP00000360615.3:n.-362_-360del
ENST00000371561.7:c.-362_-360del ENSP00000360616.3:n.-362_-360del
XM_005266073.3:c.-362_-360del XP_005266130.1:n.-362_-360del
XM_005266073.4:c.-362_-360del XP_005266130.1:n.-362_-360del