Canonical Allele Identifier: CA2692774170

Gene: GRIN1

Linked Data

• gnomAD v4: 9-137139343-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137139343_137139344insC , CM000671.2:g.137139343_137139344insC	GRCh38
NC_000009.11:g.140033795_140033796insC , CM000671.1:g.140033795_140033796insC	GRCh37
NC_000009.10:g.139153616_139153617insC	NCBI36
NG_011507.1:g.5187_5188insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371553.8:c.-144_-143insC	ENSP00000360608.3:n.-144_-143insC
ENST00000371560.5:c.-144_-143insC	ENSP00000360615.3:n.-144_-143insC
ENST00000371561.8:c.-144_-143insC MANE Select	ENSP00000360616.3:n.-144_-143insC
ENST00000350902.9:c.-144_-143insC	ENSP00000316915.9:n.-144_-143insC
ENST00000371561.7:c.-144_-143insC	ENSP00000360616.3:n.-144_-143insC
NM_000832.6:c.-144_-143insC	NP_000823.4:n.-144_-143insC
NM_001185090.1:c.-144_-143insC	NP_001172019.1:n.-144_-143insC
NM_001185091.1:c.-144_-143insC	NP_001172020.1:n.-144_-143insC
NM_007327.3:c.-144_-143insC	NP_015566.1:n.-144_-143insC
NM_021569.3:c.-144_-143insC	NP_067544.1:n.-144_-143insC
XM_005266071.2:c.-144_-143insC	XP_005266128.1:n.-144_-143insC
XM_005266072.2:c.-144_-143insC	XP_005266129.1:n.-144_-143insC
XM_005266073.3:c.-144_-143insC	XP_005266130.1:n.-144_-143insC
XM_011518583.1:c.-144_-143insC	XP_011516885.1:n.-144_-143insC
XM_005266072.3:c.-144_-143insC	XP_005266129.1:n.-144_-143insC
XM_005266073.4:c.-144_-143insC	XP_005266130.1:n.-144_-143insC
XM_011518583.2:c.-144_-143insC	XP_011516885.1:n.-144_-143insC
NM_007327.4:c.-144_-143insC MANE Select	NP_015566.1:n.-144_-143insC
NM_000832.7:c.-144_-143insC	NP_000823.4:n.-144_-143insC
NM_001185090.2:c.-144_-143insC	NP_001172019.1:n.-144_-143insC
NM_001185091.2:c.-144_-143insC	NP_001172020.1:n.-144_-143insC
NM_021569.4:c.-144_-143insC	NP_067544.1:n.-144_-143insC