Canonical Allele Identifier: CA1884320467

Gene: GRIN1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137143890_137143891delinsAG , CM000671.2:g.137143890_137143891delinsAG	GRCh38
NC_000009.11:g.140038342_140038343delinsAG , CM000671.1:g.140038342_140038343delinsAG	GRCh37
NC_000009.10:g.139158163_139158164delinsAG	NCBI36
NG_011507.1:g.9734_9735delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371553.8:c.393+1743_393+1744delinsAG	ENSP00000360608.3:n.393+1743_393+1744delinsAG
ENST00000371560.5:c.393+1743_393+1744delinsAG	ENSP00000360615.3:n.393+1743_393+1744delinsAG
ENST00000371561.8:c.393+1743_393+1744delinsAG MANE Select	ENSP00000360616.3:n.393+1743_393+1744delinsAG
ENST00000350902.9:c.393+1743_393+1744delinsAG	ENSP00000316915.9:n.393+1743_393+1744delinsAG
ENST00000371546.8:c.393+1743_393+1744delinsAG	ENSP00000360601.4:n.393+1743_393+1744delinsAG
ENST00000371550.8:c.393+1743_393+1744delinsAG	ENSP00000360605.4:n.393+1743_393+1744delinsAG
ENST00000371553.7:c.393+1743_393+1744delinsAG	ENSP00000360608.3:n.393+1743_393+1744delinsAG
ENST00000371555.8:c.393+1743_393+1744delinsAG	ENSP00000360610.4:n.393+1743_393+1744delinsAG
ENST00000371559.8:c.393+1743_393+1744delinsAG	ENSP00000360614.4:n.393+1743_393+1744delinsAG
ENST00000371560.4:c.393+1743_393+1744delinsAG	ENSP00000360615.3:n.393+1743_393+1744delinsAG
ENST00000371561.7:c.393+1743_393+1744delinsAG	ENSP00000360616.3:n.393+1743_393+1744delinsAG
ENST00000471122.5:n.470+1743_470+1744delinsAG
NM_000832.6:c.393+1743_393+1744delinsAG	NP_000823.4:n.393+1743_393+1744delinsAG
NM_001185090.1:c.393+1743_393+1744delinsAG	NP_001172019.1:n.393+1743_393+1744delinsAG
NM_001185091.1:c.393+1743_393+1744delinsAG	NP_001172020.1:n.393+1743_393+1744delinsAG
NM_007327.3:c.393+1743_393+1744delinsAG	NP_015566.1:n.393+1743_393+1744delinsAG
NM_021569.3:c.393+1743_393+1744delinsAG	NP_067544.1:n.393+1743_393+1744delinsAG
XM_005266071.2:c.393+1743_393+1744delinsAG	XP_005266128.1:n.393+1743_393+1744delinsAG
XM_005266072.2:c.393+1743_393+1744delinsAG	XP_005266129.1:n.393+1743_393+1744delinsAG
XM_005266073.3:c.393+1743_393+1744delinsAG	XP_005266130.1:n.393+1743_393+1744delinsAG
XM_011518583.1:c.393+1743_393+1744delinsAG	XP_011516885.1:n.393+1743_393+1744delinsAG
XM_005266071.3:c.393+1743_393+1744delinsAG	XP_005266128.1:n.393+1743_393+1744delinsAG
XM_005266072.3:c.393+1743_393+1744delinsAG	XP_005266129.1:n.393+1743_393+1744delinsAG
XM_005266073.4:c.393+1743_393+1744delinsAG	XP_005266130.1:n.393+1743_393+1744delinsAG
XM_011518583.2:c.393+1743_393+1744delinsAG	XP_011516885.1:n.393+1743_393+1744delinsAG
NM_007327.4:c.393+1743_393+1744delinsAG MANE Select	NP_015566.1:n.393+1743_393+1744delinsAG
NM_000832.7:c.393+1743_393+1744delinsAG	NP_000823.4:n.393+1743_393+1744delinsAG
NM_001185090.2:c.393+1743_393+1744delinsAG	NP_001172019.1:n.393+1743_393+1744delinsAG
NM_001185091.2:c.393+1743_393+1744delinsAG	NP_001172020.1:n.393+1743_393+1744delinsAG
NM_021569.4:c.393+1743_393+1744delinsAG	NP_067544.1:n.393+1743_393+1744delinsAG