Canonical Allele Identifier: CA2692777265
Gene: GRIN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137158301_137158326dup , CM000671.2:g.137158301_137158326dup GRCh38
NC_000009.11:g.140052753_140052778dup , CM000671.1:g.140052753_140052778dup GRCh37
NC_000009.10:g.139172574_139172599dup NCBI36
NG_011507.1:g.24145_24170dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000371553.8:c.1032-78_1032-53dup ENSP00000360608.3:n.1032-78_1032-53dup
ENST00000371560.5:c.1032-78_1032-53dup ENSP00000360615.3:n.1032-78_1032-53dup
ENST00000371561.8:c.969-78_969-53dup MANE Select ENSP00000360616.3:n.969-78_969-53dup
ENST00000675295.1:n.399-78_399-53dup
ENST00000676396.1:n.2479-78_2479-53dup
ENST00000350902.9:c.1015-78_1015-53dup ENSP00000316915.9:n.1015-78_1015-53dup
ENST00000371546.8:c.1032-78_1032-53dup ENSP00000360601.4:n.1032-78_1032-53dup
ENST00000371550.8:c.969-78_969-53dup ENSP00000360605.4:n.969-78_969-53dup
ENST00000371553.7:c.1032-78_1032-53dup ENSP00000360608.3:n.1032-78_1032-53dup
ENST00000371555.8:c.1032-78_1032-53dup ENSP00000360610.4:n.1032-78_1032-53dup
ENST00000371559.8:c.969-78_969-53dup ENSP00000360614.4:n.969-78_969-53dup
ENST00000371560.4:c.1032-78_1032-53dup ENSP00000360615.3:n.1032-78_1032-53dup
ENST00000371561.7:c.969-78_969-53dup ENSP00000360616.3:n.969-78_969-53dup
ENST00000471122.5:n.1046-78_1046-53dup
ENST00000485413.1:n.63-78_63-53dup
NM_000832.6:c.969-78_969-53dup NP_000823.4:n.969-78_969-53dup
NM_001185090.1:c.1032-78_1032-53dup NP_001172019.1:n.1032-78_1032-53dup
NM_001185091.1:c.1032-78_1032-53dup NP_001172020.1:n.1032-78_1032-53dup
NM_007327.3:c.969-78_969-53dup NP_015566.1:n.969-78_969-53dup
NM_021569.3:c.969-78_969-53dup NP_067544.1:n.969-78_969-53dup
XM_005266071.2:c.969-78_969-53dup XP_005266128.1:n.969-78_969-53dup
XM_005266072.2:c.1032-78_1032-53dup XP_005266129.1:n.1032-78_1032-53dup
XM_005266073.3:c.1032-78_1032-53dup XP_005266130.1:n.1032-78_1032-53dup
XM_011518583.1:c.1032-78_1032-53dup XP_011516885.1:n.1032-78_1032-53dup
XM_005266071.3:c.969-78_969-53dup XP_005266128.1:n.969-78_969-53dup
XM_005266072.3:c.1032-78_1032-53dup XP_005266129.1:n.1032-78_1032-53dup
XM_005266073.4:c.1032-78_1032-53dup XP_005266130.1:n.1032-78_1032-53dup
XM_011518583.2:c.1032-78_1032-53dup XP_011516885.1:n.1032-78_1032-53dup
NM_007327.4:c.969-78_969-53dup MANE Select NP_015566.1:n.969-78_969-53dup
NM_000832.7:c.969-78_969-53dup NP_000823.4:n.969-78_969-53dup
NM_001185090.2:c.1032-78_1032-53dup NP_001172019.1:n.1032-78_1032-53dup
NM_001185091.2:c.1032-78_1032-53dup NP_001172020.1:n.1032-78_1032-53dup
NM_021569.4:c.969-78_969-53dup NP_067544.1:n.969-78_969-53dup