Canonical Allele Identifier: CA591372820

Gene: GRIN1

Linked Data

• dbSNP Id: rs1428930734
• gnomAD v2: 9-140056787-G-GGTT
• gnomAD v4: 9-137162335-G-GGTT
• MyVariant Identifiers: chr9:g.140056787_140056788insGTT (hg19) ; chr9:g.137162335_137162336insGTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137162335_137162336insGTT , CM000671.2:g.137162335_137162336insGTT	GRCh38
NC_000009.11:g.140056787_140056788insGTT , CM000671.1:g.140056787_140056788insGTT	GRCh37
NC_000009.10:g.139176608_139176609insGTT	NCBI36
NG_011507.1:g.28179_28180insGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371553.8:c.1814+45_1814+46insGTT	ENSP00000360608.3:n.1814+45_1814+46insGTT
ENST00000371560.5:c.1814+45_1814+46insGTT	ENSP00000360615.3:n.1814+45_1814+46insGTT
ENST00000371561.8:c.1751+45_1751+46insGTT MANE Select	ENSP00000360616.3:n.1751+45_1751+46insGTT
ENST00000675295.1:n.1181+45_1181+46insGTT
ENST00000350902.9:c.*726+45_*726+46insGTT	ENSP00000316915.9:n.*726+45_*726+46insGTT
ENST00000371546.8:c.1814+45_1814+46insGTT	ENSP00000360601.4:n.1814+45_1814+46insGTT
ENST00000371550.8:c.1751+45_1751+46insGTT	ENSP00000360605.4:n.1751+45_1751+46insGTT
ENST00000371553.7:c.1814+45_1814+46insGTT	ENSP00000360608.3:n.1814+45_1814+46insGTT
ENST00000371555.8:c.1814+45_1814+46insGTT	ENSP00000360610.4:n.1814+45_1814+46insGTT
ENST00000371559.8:c.1751+45_1751+46insGTT	ENSP00000360614.4:n.1751+45_1751+46insGTT
ENST00000371560.4:c.1814+45_1814+46insGTT	ENSP00000360615.3:n.1814+45_1814+46insGTT
ENST00000371561.7:c.1751+45_1751+46insGTT	ENSP00000360616.3:n.1751+45_1751+46insGTT
ENST00000471122.5:n.1828+45_1828+46insGTT
NM_000832.6:c.1751+45_1751+46insGTT	NP_000823.4:n.1751+45_1751+46insGTT
NM_001185090.1:c.1814+45_1814+46insGTT	NP_001172019.1:n.1814+45_1814+46insGTT
NM_001185091.1:c.1814+45_1814+46insGTT	NP_001172020.1:n.1814+45_1814+46insGTT
NM_007327.3:c.1751+45_1751+46insGTT	NP_015566.1:n.1751+45_1751+46insGTT
NM_021569.3:c.1751+45_1751+46insGTT	NP_067544.1:n.1751+45_1751+46insGTT
XM_005266071.2:c.1751+45_1751+46insGTT	XP_005266128.1:n.1751+45_1751+46insGTT
XM_005266072.2:c.1814+45_1814+46insGTT	XP_005266129.1:n.1814+45_1814+46insGTT
XM_005266073.3:c.1814+45_1814+46insGTT	XP_005266130.1:n.1814+45_1814+46insGTT
XM_011518583.1:c.1814+45_1814+46insGTT	XP_011516885.1:n.1814+45_1814+46insGTT
XM_005266071.3:c.1751+45_1751+46insGTT	XP_005266128.1:n.1751+45_1751+46insGTT
XM_005266072.3:c.1814+45_1814+46insGTT	XP_005266129.1:n.1814+45_1814+46insGTT
XM_005266073.4:c.1814+45_1814+46insGTT	XP_005266130.1:n.1814+45_1814+46insGTT
XM_011518583.2:c.1814+45_1814+46insGTT	XP_011516885.1:n.1814+45_1814+46insGTT
NM_007327.4:c.1751+45_1751+46insGTT MANE Select	NP_015566.1:n.1751+45_1751+46insGTT
NM_000832.7:c.1751+45_1751+46insGTT	NP_000823.4:n.1751+45_1751+46insGTT
NM_001185090.2:c.1814+45_1814+46insGTT	NP_001172019.1:n.1814+45_1814+46insGTT
NM_001185091.2:c.1814+45_1814+46insGTT	NP_001172020.1:n.1814+45_1814+46insGTT
NM_021569.4:c.1751+45_1751+46insGTT	NP_067544.1:n.1751+45_1751+46insGTT