Canonical Allele Identifier: CA2692781689
Gene: GRIN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137162116_137162117insTGGGGGGGGGGGGGGGGGGGGG , CM000671.2:g.137162116_137162117insTGGGGGGGGGGGGGGGGGGGGG GRCh38
NC_000009.11:g.140056568_140056569insTGGGGGGGGGGGGGGGGGGGGG , CM000671.1:g.140056568_140056569insTGGGGGGGGGGGGGGGGGGGGG GRCh37
NC_000009.10:g.139176389_139176390insTGGGGGGGGGGGGGGGGGGGGG NCBI36
NG_011507.1:g.27960_27961insTGGGGGGGGGGGGGGGGGGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000371553.8:c.1695+28_1695+29insTGGGGGGGGGGGGGGGGGGGGG ENSP00000360608.3:n.1695+28_1695+29insTGGGGGGGGGGGGGGGGGGGGG
ENST00000371560.5:c.1695+28_1695+29insTGGGGGGGGGGGGGGGGGGGGG ENSP00000360615.3:n.1695+28_1695+29insTGGGGGGGGGGGGGGGGGGGGG
ENST00000371561.8:c.1632+28_1632+29insTGGGGGGGGGGGGGGGGGGGGG MANE Select ENSP00000360616.3:n.1632+28_1632+29insTGGGGGGGGGGGGGGGGGGGGG
ENST00000675295.1:n.1062+28_1062+29insTGGGGGGGGGGGGGGGGGGGGG
ENST00000350902.9:c.*607+28_*607+29insTGGGGGGGGGGGGGGGGGGGGG ENSP00000316915.9:n.*607+28_*607+29insTGGGGGGGGGGGGGGGGGGGGG
ENST00000371546.8:c.1695+28_1695+29insTGGGGGGGGGGGGGGGGGGGGG ENSP00000360601.4:n.1695+28_1695+29insTGGGGGGGGGGGGGGGGGGGGG
ENST00000371550.8:c.1632+28_1632+29insTGGGGGGGGGGGGGGGGGGGGG ENSP00000360605.4:n.1632+28_1632+29insTGGGGGGGGGGGGGGGGGGGGG
ENST00000371553.7:c.1695+28_1695+29insTGGGGGGGGGGGGGGGGGGGGG ENSP00000360608.3:n.1695+28_1695+29insTGGGGGGGGGGGGGGGGGGGGG
ENST00000371555.8:c.1695+28_1695+29insTGGGGGGGGGGGGGGGGGGGGG ENSP00000360610.4:n.1695+28_1695+29insTGGGGGGGGGGGGGGGGGGGGG
ENST00000371559.8:c.1632+28_1632+29insTGGGGGGGGGGGGGGGGGGGGG ENSP00000360614.4:n.1632+28_1632+29insTGGGGGGGGGGGGGGGGGGGGG
ENST00000371560.4:c.1695+28_1695+29insTGGGGGGGGGGGGGGGGGGGGG ENSP00000360615.3:n.1695+28_1695+29insTGGGGGGGGGGGGGGGGGGGGG
ENST00000371561.7:c.1632+28_1632+29insTGGGGGGGGGGGGGGGGGGGGG ENSP00000360616.3:n.1632+28_1632+29insTGGGGGGGGGGGGGGGGGGGGG
ENST00000471122.5:n.1709+28_1709+29insTGGGGGGGGGGGGGGGGGGGGG
NM_000832.6:c.1632+28_1632+29insTGGGGGGGGGGGGGGGGGGGGG NP_000823.4:n.1632+28_1632+29insTGGGGGGGGGGGGGGGGGGGGG
NM_001185090.1:c.1695+28_1695+29insTGGGGGGGGGGGGGGGGGGGGG NP_001172019.1:n.1695+28_1695+29insTGGGGGGGGGGGGGGGGGGGGG
NM_001185091.1:c.1695+28_1695+29insTGGGGGGGGGGGGGGGGGGGGG NP_001172020.1:n.1695+28_1695+29insTGGGGGGGGGGGGGGGGGGGGG
NM_007327.3:c.1632+28_1632+29insTGGGGGGGGGGGGGGGGGGGGG NP_015566.1:n.1632+28_1632+29insTGGGGGGGGGGGGGGGGGGGGG
NM_021569.3:c.1632+28_1632+29insTGGGGGGGGGGGGGGGGGGGGG NP_067544.1:n.1632+28_1632+29insTGGGGGGGGGGGGGGGGGGGGG
XM_005266071.2:c.1632+28_1632+29insTGGGGGGGGGGGGGGGGGGGGG XP_005266128.1:n.1632+28_1632+29insTGGGGGGGGGGGGGGGGGGGGG
XM_005266072.2:c.1695+28_1695+29insTGGGGGGGGGGGGGGGGGGGGG XP_005266129.1:n.1695+28_1695+29insTGGGGGGGGGGGGGGGGGGGGG
XM_005266073.3:c.1695+28_1695+29insTGGGGGGGGGGGGGGGGGGGGG XP_005266130.1:n.1695+28_1695+29insTGGGGGGGGGGGGGGGGGGGGG
XM_011518583.1:c.1695+28_1695+29insTGGGGGGGGGGGGGGGGGGGGG XP_011516885.1:n.1695+28_1695+29insTGGGGGGGGGGGGGGGGGGGGG
XM_005266071.3:c.1632+28_1632+29insTGGGGGGGGGGGGGGGGGGGGG XP_005266128.1:n.1632+28_1632+29insTGGGGGGGGGGGGGGGGGGGGG
XM_005266072.3:c.1695+28_1695+29insTGGGGGGGGGGGGGGGGGGGGG XP_005266129.1:n.1695+28_1695+29insTGGGGGGGGGGGGGGGGGGGGG
XM_005266073.4:c.1695+28_1695+29insTGGGGGGGGGGGGGGGGGGGGG XP_005266130.1:n.1695+28_1695+29insTGGGGGGGGGGGGGGGGGGGGG
XM_011518583.2:c.1695+28_1695+29insTGGGGGGGGGGGGGGGGGGGGG XP_011516885.1:n.1695+28_1695+29insTGGGGGGGGGGGGGGGGGGGGG
NM_007327.4:c.1632+28_1632+29insTGGGGGGGGGGGGGGGGGGGGG MANE Select NP_015566.1:n.1632+28_1632+29insTGGGGGGGGGGGGGGGGGGGGG
NM_000832.7:c.1632+28_1632+29insTGGGGGGGGGGGGGGGGGGGGG NP_000823.4:n.1632+28_1632+29insTGGGGGGGGGGGGGGGGGGGGG
NM_001185090.2:c.1695+28_1695+29insTGGGGGGGGGGGGGGGGGGGGG NP_001172019.1:n.1695+28_1695+29insTGGGGGGGGGGGGGGGGGGGGG
NM_001185091.2:c.1695+28_1695+29insTGGGGGGGGGGGGGGGGGGGGG NP_001172020.1:n.1695+28_1695+29insTGGGGGGGGGGGGGGGGGGGGG
NM_021569.4:c.1632+28_1632+29insTGGGGGGGGGGGGGGGGGGGGG NP_067544.1:n.1632+28_1632+29insTGGGGGGGGGGGGGGGGGGGGG