Canonical Allele Identifier: CA2692781775
Gene: GRIN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137162125_137162126insGGGGGTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG , CM000671.2:g.137162125_137162126insGGGGGTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG GRCh38
NC_000009.11:g.140056577_140056578insGGGGGTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG , CM000671.1:g.140056577_140056578insGGGGGTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG GRCh37
NC_000009.10:g.139176398_139176399insGGGGGTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG NCBI36
NG_011507.1:g.27969_27970insGGGGGTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000371553.8:c.1695+37_1695+38insGGGGGTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG ENSP00000360608.3:n.1695+37_1695+38insGGGGGTGGGGGGGGGGGGGGGGG...
ENST00000371560.5:c.1695+37_1695+38insGGGGGTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG ENSP00000360615.3:n.1695+37_1695+38insGGGGGTGGGGGGGGGGGGGGGGG...
ENST00000371561.8:c.1632+37_1632+38insGGGGGTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG MANE Select ENSP00000360616.3:n.1632+37_1632+38insGGGGGTGGGGGGGGGGGGGGGGG...
ENST00000675295.1:n.1062+37_1062+38insGGGGGTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG
ENST00000350902.9:c.*607+37_*607+38insGGGGGTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG ENSP00000316915.9:n.*607+37_*607+38insGGGGGTGGGGGGGGGGGGGGGGG...
ENST00000371546.8:c.1695+37_1695+38insGGGGGTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG ENSP00000360601.4:n.1695+37_1695+38insGGGGGTGGGGGGGGGGGGGGGGG...
ENST00000371550.8:c.1632+37_1632+38insGGGGGTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG ENSP00000360605.4:n.1632+37_1632+38insGGGGGTGGGGGGGGGGGGGGGGG...
ENST00000371553.7:c.1695+37_1695+38insGGGGGTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG ENSP00000360608.3:n.1695+37_1695+38insGGGGGTGGGGGGGGGGGGGGGGG...
ENST00000371555.8:c.1695+37_1695+38insGGGGGTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG ENSP00000360610.4:n.1695+37_1695+38insGGGGGTGGGGGGGGGGGGGGGGG...
ENST00000371559.8:c.1632+37_1632+38insGGGGGTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG ENSP00000360614.4:n.1632+37_1632+38insGGGGGTGGGGGGGGGGGGGGGGG...
ENST00000371560.4:c.1695+37_1695+38insGGGGGTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG ENSP00000360615.3:n.1695+37_1695+38insGGGGGTGGGGGGGGGGGGGGGGG...
ENST00000371561.7:c.1632+37_1632+38insGGGGGTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG ENSP00000360616.3:n.1632+37_1632+38insGGGGGTGGGGGGGGGGGGGGGGG...
ENST00000471122.5:n.1709+37_1709+38insGGGGGTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG
NM_000832.6:c.1632+37_1632+38insGGGGGTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG NP_000823.4:n.1632+37_1632+38insGGGGGTGGGGGGGGGGGGGGGGGGGGGGG...
NM_001185090.1:c.1695+37_1695+38insGGGGGTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG NP_001172019.1:n.1695+37_1695+38insGGGGGTGGGGGGGGGGGGGGGGGGGG...
NM_001185091.1:c.1695+37_1695+38insGGGGGTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG NP_001172020.1:n.1695+37_1695+38insGGGGGTGGGGGGGGGGGGGGGGGGGG...
NM_007327.3:c.1632+37_1632+38insGGGGGTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG NP_015566.1:n.1632+37_1632+38insGGGGGTGGGGGGGGGGGGGGGGGGGGGGG...
NM_021569.3:c.1632+37_1632+38insGGGGGTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG NP_067544.1:n.1632+37_1632+38insGGGGGTGGGGGGGGGGGGGGGGGGGGGGG...
XM_005266071.2:c.1632+37_1632+38insGGGGGTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG XP_005266128.1:n.1632+37_1632+38insGGGGGTGGGGGGGGGGGGGGGGGGGG...
XM_005266072.2:c.1695+37_1695+38insGGGGGTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG XP_005266129.1:n.1695+37_1695+38insGGGGGTGGGGGGGGGGGGGGGGGGGG...
XM_005266073.3:c.1695+37_1695+38insGGGGGTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG XP_005266130.1:n.1695+37_1695+38insGGGGGTGGGGGGGGGGGGGGGGGGGG...
XM_011518583.1:c.1695+37_1695+38insGGGGGTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG XP_011516885.1:n.1695+37_1695+38insGGGGGTGGGGGGGGGGGGGGGGGGGG...
XM_005266071.3:c.1632+37_1632+38insGGGGGTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG XP_005266128.1:n.1632+37_1632+38insGGGGGTGGGGGGGGGGGGGGGGGGGG...
XM_005266072.3:c.1695+37_1695+38insGGGGGTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG XP_005266129.1:n.1695+37_1695+38insGGGGGTGGGGGGGGGGGGGGGGGGGG...
XM_005266073.4:c.1695+37_1695+38insGGGGGTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG XP_005266130.1:n.1695+37_1695+38insGGGGGTGGGGGGGGGGGGGGGGGGGG...
XM_011518583.2:c.1695+37_1695+38insGGGGGTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG XP_011516885.1:n.1695+37_1695+38insGGGGGTGGGGGGGGGGGGGGGGGGGG...
NM_007327.4:c.1632+37_1632+38insGGGGGTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG MANE Select NP_015566.1:n.1632+37_1632+38insGGGGGTGGGGGGGGGGGGGGGGGGGGGGG...
NM_000832.7:c.1632+37_1632+38insGGGGGTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG NP_000823.4:n.1632+37_1632+38insGGGGGTGGGGGGGGGGGGGGGGGGGGGGG...
NM_001185090.2:c.1695+37_1695+38insGGGGGTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG NP_001172019.1:n.1695+37_1695+38insGGGGGTGGGGGGGGGGGGGGGGGGGG...
NM_001185091.2:c.1695+37_1695+38insGGGGGTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG NP_001172020.1:n.1695+37_1695+38insGGGGGTGGGGGGGGGGGGGGGGGGGG...
NM_021569.4:c.1632+37_1632+38insGGGGGTGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG NP_067544.1:n.1632+37_1632+38insGGGGGTGGGGGGGGGGGGGGGGGGGGGGG...