Canonical Allele Identifier: CA591373339

Gene: GRIN1

Linked Data

• gnomAD v2: 9-140056560-C-CGGGGGGGG
• gnomAD v3: 9-137162108-C-CGGGGGGGG
• gnomAD v4: 9-137162108-C-CGGGGGGGG
• MyVariant Identifiers: chr9:g.140056560_140056561insGGGGGGGG (hg19) ; chr9:g.137162108_137162109insGGGGGGGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137162112_137162113insGGGGGGGG , CM000671.2:g.137162112_137162113insGGGGGGGG	GRCh38
NC_000009.11:g.140056564_140056565insGGGGGGGG , CM000671.1:g.140056564_140056565insGGGGGGGG	GRCh37
NC_000009.10:g.139176385_139176386insGGGGGGGG	NCBI36
NG_011507.1:g.27956_27957insGGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371553.8:c.1695+24_1695+25insGGGGGGGG	ENSP00000360608.3:n.1695+24_1695+25insGGGGGGGG
ENST00000371560.5:c.1695+24_1695+25insGGGGGGGG	ENSP00000360615.3:n.1695+24_1695+25insGGGGGGGG
ENST00000371561.8:c.1632+24_1632+25insGGGGGGGG MANE Select	ENSP00000360616.3:n.1632+24_1632+25insGGGGGGGG
ENST00000675295.1:n.1062+24_1062+25insGGGGGGGG
ENST00000350902.9:c.*607+24_*607+25insGGGGGGGG	ENSP00000316915.9:n.*607+24_*607+25insGGGGGGGG
ENST00000371546.8:c.1695+24_1695+25insGGGGGGGG	ENSP00000360601.4:n.1695+24_1695+25insGGGGGGGG
ENST00000371550.8:c.1632+24_1632+25insGGGGGGGG	ENSP00000360605.4:n.1632+24_1632+25insGGGGGGGG
ENST00000371553.7:c.1695+24_1695+25insGGGGGGGG	ENSP00000360608.3:n.1695+24_1695+25insGGGGGGGG
ENST00000371555.8:c.1695+24_1695+25insGGGGGGGG	ENSP00000360610.4:n.1695+24_1695+25insGGGGGGGG
ENST00000371559.8:c.1632+24_1632+25insGGGGGGGG	ENSP00000360614.4:n.1632+24_1632+25insGGGGGGGG
ENST00000371560.4:c.1695+24_1695+25insGGGGGGGG	ENSP00000360615.3:n.1695+24_1695+25insGGGGGGGG
ENST00000371561.7:c.1632+24_1632+25insGGGGGGGG	ENSP00000360616.3:n.1632+24_1632+25insGGGGGGGG
ENST00000471122.5:n.1709+24_1709+25insGGGGGGGG
NM_000832.6:c.1632+24_1632+25insGGGGGGGG	NP_000823.4:n.1632+24_1632+25insGGGGGGGG
NM_001185090.1:c.1695+24_1695+25insGGGGGGGG	NP_001172019.1:n.1695+24_1695+25insGGGGGGGG
NM_001185091.1:c.1695+24_1695+25insGGGGGGGG	NP_001172020.1:n.1695+24_1695+25insGGGGGGGG
NM_007327.3:c.1632+24_1632+25insGGGGGGGG	NP_015566.1:n.1632+24_1632+25insGGGGGGGG
NM_021569.3:c.1632+24_1632+25insGGGGGGGG	NP_067544.1:n.1632+24_1632+25insGGGGGGGG
XM_005266071.2:c.1632+24_1632+25insGGGGGGGG	XP_005266128.1:n.1632+24_1632+25insGGGGGGGG
XM_005266072.2:c.1695+24_1695+25insGGGGGGGG	XP_005266129.1:n.1695+24_1695+25insGGGGGGGG
XM_005266073.3:c.1695+24_1695+25insGGGGGGGG	XP_005266130.1:n.1695+24_1695+25insGGGGGGGG
XM_011518583.1:c.1695+24_1695+25insGGGGGGGG	XP_011516885.1:n.1695+24_1695+25insGGGGGGGG
XM_005266071.3:c.1632+24_1632+25insGGGGGGGG	XP_005266128.1:n.1632+24_1632+25insGGGGGGGG
XM_005266072.3:c.1695+24_1695+25insGGGGGGGG	XP_005266129.1:n.1695+24_1695+25insGGGGGGGG
XM_005266073.4:c.1695+24_1695+25insGGGGGGGG	XP_005266130.1:n.1695+24_1695+25insGGGGGGGG
XM_011518583.2:c.1695+24_1695+25insGGGGGGGG	XP_011516885.1:n.1695+24_1695+25insGGGGGGGG
NM_007327.4:c.1632+24_1632+25insGGGGGGGG MANE Select	NP_015566.1:n.1632+24_1632+25insGGGGGGGG
NM_000832.7:c.1632+24_1632+25insGGGGGGGG	NP_000823.4:n.1632+24_1632+25insGGGGGGGG
NM_001185090.2:c.1695+24_1695+25insGGGGGGGG	NP_001172019.1:n.1695+24_1695+25insGGGGGGGG
NM_001185091.2:c.1695+24_1695+25insGGGGGGGG	NP_001172020.1:n.1695+24_1695+25insGGGGGGGG
NM_021569.4:c.1632+24_1632+25insGGGGGGGG	NP_067544.1:n.1632+24_1632+25insGGGGGGGG