Canonical Allele Identifier: CA1884333342
Gene: GRIN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137167481G= , CM000671.2:g.137167481G= GRCh38
NC_000009.11:g.140061933G= , CM000671.1:g.140061933G= GRCh37
NC_000009.10:g.139181754G= NCBI36
NG_011507.1:g.33325G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371553.8:c.2764-293G= ENSP00000360608.3:n.2764-293G=
ENST00000371560.5:c.2653-293G= ENSP00000360615.3:n.2653-293G=
ENST00000371561.8:c.2771G= MANE Select ENSP00000360616.3:p.Arg924=
ENST00000371546.8:c.2834G= ENSP00000360601.4:p.Arg945=
ENST00000371550.8:c.2660G= ENSP00000360605.4:p.Arg887=
ENST00000371553.7:c.2764-293G= ENSP00000360608.3:n.2764-293G=
ENST00000371555.8:c.2723G= ENSP00000360610.4:p.Arg908=
ENST00000371559.8:c.2590-293G= ENSP00000360614.4:n.2590-293G=
ENST00000371560.4:c.2653-293G= ENSP00000360615.3:n.2653-293G=
ENST00000371561.7:c.2771G= ENSP00000360616.3:p.Arg924=
ENST00000473811.1:n.251G=
NM_000832.6:c.2590-293G= NP_000823.4:n.2590-293G=
NM_001185090.1:c.2764-293G= NP_001172019.1:n.2764-293G=
NM_001185091.1:c.2653-293G= NP_001172020.1:n.2653-293G=
NM_007327.3:c.2771G= NP_015566.1:p.Arg924=
NM_021569.3:c.2660G= NP_067544.1:p.Arg887=
XM_005266071.2:c.2701-293G= XP_005266128.1:n.2701-293G=
XM_005266072.2:c.2723G= XP_005266129.1:p.Arg908=
XM_005266073.3:c.2834G= XP_005266130.1:p.Arg945=
XM_005266071.3:c.2701-293G= XP_005266128.1:n.2701-293G=
XM_005266072.3:c.2723G= XP_005266129.1:p.Arg908=
XM_005266073.4:c.2834G= XP_005266130.1:p.Arg945=
NM_007327.4:c.2771G= MANE Select NP_015566.1:p.Arg924=
NM_000832.7:c.2590-293G= NP_000823.4:n.2590-293G=
NM_001185090.2:c.2764-293G= NP_001172019.1:n.2764-293G=
NM_001185091.2:c.2653-293G= NP_001172020.1:n.2653-293G=
NM_021569.4:c.2660G= NP_067544.1:p.Arg887=