Canonical Allele Identifier: CA375729649
Gene: GRIN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137167442A>G , CM000671.2:g.137167442A>G GRCh38
NC_000009.11:g.140061894A>G , CM000671.1:g.140061894A>G GRCh37
NC_000009.10:g.139181715A>G NCBI36
NG_011507.1:g.33286A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371553.8:c.2764-332A>G ENSP00000360608.3:n.2764-332A>G
ENST00000371560.5:c.2653-332A>G ENSP00000360615.3:n.2653-332A>G
ENST00000371561.8:c.2732A>G MANE Select ENSP00000360616.3:p.Asn911Ser
ENST00000371546.8:c.2795A>G ENSP00000360601.4:p.Asn932Ser
ENST00000371550.8:c.2621A>G ENSP00000360605.4:p.Asn874Ser
ENST00000371553.7:c.2764-332A>G ENSP00000360608.3:n.2764-332A>G
ENST00000371555.8:c.2684A>G ENSP00000360610.4:p.Asn895Ser
ENST00000371559.8:c.2590-332A>G ENSP00000360614.4:n.2590-332A>G
ENST00000371560.4:c.2653-332A>G ENSP00000360615.3:n.2653-332A>G
ENST00000371561.7:c.2732A>G ENSP00000360616.3:p.Asn911Ser
ENST00000473811.1:n.212A>G
NM_000832.6:c.2590-332A>G NP_000823.4:n.2590-332A>G
NM_001185090.1:c.2764-332A>G NP_001172019.1:n.2764-332A>G
NM_001185091.1:c.2653-332A>G NP_001172020.1:n.2653-332A>G
NM_007327.3:c.2732A>G NP_015566.1:p.Asn911Ser
NM_021569.3:c.2621A>G NP_067544.1:p.Asn874Ser
XM_005266071.2:c.2701-332A>G XP_005266128.1:n.2701-332A>G
XM_005266072.2:c.2684A>G XP_005266129.1:p.Asn895Ser
XM_005266073.3:c.2795A>G XP_005266130.1:p.Asn932Ser
XM_005266071.3:c.2701-332A>G XP_005266128.1:n.2701-332A>G
XM_005266072.3:c.2684A>G XP_005266129.1:p.Asn895Ser
XM_005266073.4:c.2795A>G XP_005266130.1:p.Asn932Ser
NM_007327.4:c.2732A>G MANE Select NP_015566.1:p.Asn911Ser
NM_000832.7:c.2590-332A>G NP_000823.4:n.2590-332A>G
NM_001185090.2:c.2764-332A>G NP_001172019.1:n.2764-332A>G
NM_001185091.2:c.2653-332A>G NP_001172020.1:n.2653-332A>G
NM_021569.4:c.2621A>G NP_067544.1:p.Asn874Ser