Canonical Allele Identifier: CA375729556
Gene: GRIN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137167418G>C , CM000671.2:g.137167418G>C GRCh38
NC_000009.11:g.140061870G>C , CM000671.1:g.140061870G>C GRCh37
NC_000009.10:g.139181691G>C NCBI36
NG_011507.1:g.33262G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000371553.8:c.2764-356G>C ENSP00000360608.3:n.2764-356G>C
ENST00000371560.5:c.2653-356G>C ENSP00000360615.3:n.2653-356G>C
ENST00000371561.8:c.2708G>C MANE Select ENSP00000360616.3:p.Gly903Ala
ENST00000371546.8:c.2771G>C ENSP00000360601.4:p.Gly924Ala
ENST00000371550.8:c.2597G>C ENSP00000360605.4:p.Gly866Ala
ENST00000371553.7:c.2764-356G>C ENSP00000360608.3:n.2764-356G>C
ENST00000371555.8:c.2660G>C ENSP00000360610.4:p.Gly887Ala
ENST00000371559.8:c.2590-356G>C ENSP00000360614.4:n.2590-356G>C
ENST00000371560.4:c.2653-356G>C ENSP00000360615.3:n.2653-356G>C
ENST00000371561.7:c.2708G>C ENSP00000360616.3:p.Gly903Ala
ENST00000473811.1:n.188G>C
NM_000832.6:c.2590-356G>C NP_000823.4:n.2590-356G>C
NM_001185090.1:c.2764-356G>C NP_001172019.1:n.2764-356G>C
NM_001185091.1:c.2653-356G>C NP_001172020.1:n.2653-356G>C
NM_007327.3:c.2708G>C NP_015566.1:p.Gly903Ala
NM_021569.3:c.2597G>C NP_067544.1:p.Gly866Ala
XM_005266071.2:c.2701-356G>C XP_005266128.1:n.2701-356G>C
XM_005266072.2:c.2660G>C XP_005266129.1:p.Gly887Ala
XM_005266073.3:c.2771G>C XP_005266130.1:p.Gly924Ala
XM_005266071.3:c.2701-356G>C XP_005266128.1:n.2701-356G>C
XM_005266072.3:c.2660G>C XP_005266129.1:p.Gly887Ala
XM_005266073.4:c.2771G>C XP_005266130.1:p.Gly924Ala
NM_007327.4:c.2708G>C MANE Select NP_015566.1:p.Gly903Ala
NM_000832.7:c.2590-356G>C NP_000823.4:n.2590-356G>C
NM_001185090.2:c.2764-356G>C NP_001172019.1:n.2764-356G>C
NM_001185091.2:c.2653-356G>C NP_001172020.1:n.2653-356G>C
NM_021569.4:c.2597G>C NP_067544.1:p.Gly866Ala