Canonical Allele Identifier: CA375729731
Gene: GRIN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137167463C>A , CM000671.2:g.137167463C>A GRCh38
NC_000009.11:g.140061915C>A , CM000671.1:g.140061915C>A GRCh37
NC_000009.10:g.139181736C>A NCBI36
NG_011507.1:g.33307C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371553.8:c.2764-311C>A ENSP00000360608.3:n.2764-311C>A
ENST00000371560.5:c.2653-311C>A ENSP00000360615.3:n.2653-311C>A
ENST00000371561.8:c.2753C>A MANE Select ENSP00000360616.3:p.Pro918Gln
ENST00000371546.8:c.2816C>A ENSP00000360601.4:p.Pro939Gln
ENST00000371550.8:c.2642C>A ENSP00000360605.4:p.Pro881Gln
ENST00000371553.7:c.2764-311C>A ENSP00000360608.3:n.2764-311C>A
ENST00000371555.8:c.2705C>A ENSP00000360610.4:p.Pro902Gln
ENST00000371559.8:c.2590-311C>A ENSP00000360614.4:n.2590-311C>A
ENST00000371560.4:c.2653-311C>A ENSP00000360615.3:n.2653-311C>A
ENST00000371561.7:c.2753C>A ENSP00000360616.3:p.Pro918Gln
ENST00000473811.1:n.233C>A
NM_000832.6:c.2590-311C>A NP_000823.4:n.2590-311C>A
NM_001185090.1:c.2764-311C>A NP_001172019.1:n.2764-311C>A
NM_001185091.1:c.2653-311C>A NP_001172020.1:n.2653-311C>A
NM_007327.3:c.2753C>A NP_015566.1:p.Pro918Gln
NM_021569.3:c.2642C>A NP_067544.1:p.Pro881Gln
XM_005266071.2:c.2701-311C>A XP_005266128.1:n.2701-311C>A
XM_005266072.2:c.2705C>A XP_005266129.1:p.Pro902Gln
XM_005266073.3:c.2816C>A XP_005266130.1:p.Pro939Gln
XM_005266071.3:c.2701-311C>A XP_005266128.1:n.2701-311C>A
XM_005266072.3:c.2705C>A XP_005266129.1:p.Pro902Gln
XM_005266073.4:c.2816C>A XP_005266130.1:p.Pro939Gln
NM_007327.4:c.2753C>A MANE Select NP_015566.1:p.Pro918Gln
NM_000832.7:c.2590-311C>A NP_000823.4:n.2590-311C>A
NM_001185090.2:c.2764-311C>A NP_001172019.1:n.2764-311C>A
NM_001185091.2:c.2653-311C>A NP_001172020.1:n.2653-311C>A
NM_021569.4:c.2642C>A NP_067544.1:p.Pro881Gln