Canonical Allele Identifier: CA1884330837

Gene: GRIN1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137162100_137162107delinsCCGGGTGG , CM000671.2:g.137162100_137162107delinsCCGGGTGG	GRCh38
NC_000009.11:g.140056552_140056559delinsCCGGGTGG , CM000671.1:g.140056552_140056559delinsCCGGGTGG	GRCh37
NC_000009.10:g.139176373_139176380delinsCCGGGTGG	NCBI36
NG_011507.1:g.27944_27951delinsCCGGGTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371553.8:c.1695+12_1695+19delinsCCGGGTGG	ENSP00000360608.3:n.1695+12_1695+19delinsCCGGGTGG
ENST00000371560.5:c.1695+12_1695+19delinsCCGGGTGG	ENSP00000360615.3:n.1695+12_1695+19delinsCCGGGTGG
ENST00000371561.8:c.1632+12_1632+19delinsCCGGGTGG MANE Select	ENSP00000360616.3:n.1632+12_1632+19delinsCCGGGTGG
ENST00000675295.1:n.1062+12_1062+19delinsCCGGGTGG
ENST00000350902.9:c.*607+12_*607+19delinsCCGGGTGG	ENSP00000316915.9:n.*607+12_*607+19delinsCCGGGTGG
ENST00000371546.8:c.1695+12_1695+19delinsCCGGGTGG	ENSP00000360601.4:n.1695+12_1695+19delinsCCGGGTGG
ENST00000371550.8:c.1632+12_1632+19delinsCCGGGTGG	ENSP00000360605.4:n.1632+12_1632+19delinsCCGGGTGG
ENST00000371553.7:c.1695+12_1695+19delinsCCGGGTGG	ENSP00000360608.3:n.1695+12_1695+19delinsCCGGGTGG
ENST00000371555.8:c.1695+12_1695+19delinsCCGGGTGG	ENSP00000360610.4:n.1695+12_1695+19delinsCCGGGTGG
ENST00000371559.8:c.1632+12_1632+19delinsCCGGGTGG	ENSP00000360614.4:n.1632+12_1632+19delinsCCGGGTGG
ENST00000371560.4:c.1695+12_1695+19delinsCCGGGTGG	ENSP00000360615.3:n.1695+12_1695+19delinsCCGGGTGG
ENST00000371561.7:c.1632+12_1632+19delinsCCGGGTGG	ENSP00000360616.3:n.1632+12_1632+19delinsCCGGGTGG
ENST00000471122.5:n.1709+12_1709+19delinsCCGGGTGG
NM_000832.6:c.1632+12_1632+19delinsCCGGGTGG	NP_000823.4:n.1632+12_1632+19delinsCCGGGTGG
NM_001185090.1:c.1695+12_1695+19delinsCCGGGTGG	NP_001172019.1:n.1695+12_1695+19delinsCCGGGTGG
NM_001185091.1:c.1695+12_1695+19delinsCCGGGTGG	NP_001172020.1:n.1695+12_1695+19delinsCCGGGTGG
NM_007327.3:c.1632+12_1632+19delinsCCGGGTGG	NP_015566.1:n.1632+12_1632+19delinsCCGGGTGG
NM_021569.3:c.1632+12_1632+19delinsCCGGGTGG	NP_067544.1:n.1632+12_1632+19delinsCCGGGTGG
XM_005266071.2:c.1632+12_1632+19delinsCCGGGTGG	XP_005266128.1:n.1632+12_1632+19delinsCCGGGTGG
XM_005266072.2:c.1695+12_1695+19delinsCCGGGTGG	XP_005266129.1:n.1695+12_1695+19delinsCCGGGTGG
XM_005266073.3:c.1695+12_1695+19delinsCCGGGTGG	XP_005266130.1:n.1695+12_1695+19delinsCCGGGTGG
XM_011518583.1:c.1695+12_1695+19delinsCCGGGTGG	XP_011516885.1:n.1695+12_1695+19delinsCCGGGTGG
XM_005266071.3:c.1632+12_1632+19delinsCCGGGTGG	XP_005266128.1:n.1632+12_1632+19delinsCCGGGTGG
XM_005266072.3:c.1695+12_1695+19delinsCCGGGTGG	XP_005266129.1:n.1695+12_1695+19delinsCCGGGTGG
XM_005266073.4:c.1695+12_1695+19delinsCCGGGTGG	XP_005266130.1:n.1695+12_1695+19delinsCCGGGTGG
XM_011518583.2:c.1695+12_1695+19delinsCCGGGTGG	XP_011516885.1:n.1695+12_1695+19delinsCCGGGTGG
NM_007327.4:c.1632+12_1632+19delinsCCGGGTGG MANE Select	NP_015566.1:n.1632+12_1632+19delinsCCGGGTGG
NM_000832.7:c.1632+12_1632+19delinsCCGGGTGG	NP_000823.4:n.1632+12_1632+19delinsCCGGGTGG
NM_001185090.2:c.1695+12_1695+19delinsCCGGGTGG	NP_001172019.1:n.1695+12_1695+19delinsCCGGGTGG
NM_001185091.2:c.1695+12_1695+19delinsCCGGGTGG	NP_001172020.1:n.1695+12_1695+19delinsCCGGGTGG
NM_021569.4:c.1632+12_1632+19delinsCCGGGTGG	NP_067544.1:n.1632+12_1632+19delinsCCGGGTGG