Canonical Allele Identifier: CA1884318135
Gene: GRIN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137139121G= , CM000671.2:g.137139121G= GRCh38
NC_000009.11:g.140033573G= , CM000671.1:g.140033573G= GRCh37
NC_000009.10:g.139153394G= NCBI36
NG_011507.1:g.4965G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371560.5:c.-366G= ENSP00000360615.3:n.-366G=
ENST00000371561.7:c.-366G= ENSP00000360616.3:n.-366G=
XM_005266073.3:c.-366G= XP_005266130.1:n.-366G=
XM_005266073.4:c.-366G= XP_005266130.1:n.-366G=