Canonical Allele Identifier: CA1884330884

Gene: GRIN1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137162431_137162432delinsCG , CM000671.2:g.137162431_137162432delinsCG	GRCh38
NC_000009.11:g.140056883_140056884delinsCG , CM000671.1:g.140056883_140056884delinsCG	GRCh37
NC_000009.10:g.139176704_139176705delinsCG	NCBI36
NG_011507.1:g.28275_28276delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371553.8:c.1842_1843delinsCG	ENSP00000360608.3:p.Ser614=
ENST00000371560.5:c.1842_1843delinsCG	ENSP00000360615.3:p.Ser614=
ENST00000371561.8:c.1779_1780delinsCG MANE Select	ENSP00000360616.3:p.Ser593=
ENST00000675295.1:n.1209_1210delinsCG
ENST00000350902.9:c.*754_*755delinsCG	ENSP00000316915.9:n.*754_*755delinsCG
ENST00000371546.8:c.1842_1843delinsCG	ENSP00000360601.4:p.Ser614=
ENST00000371550.8:c.1779_1780delinsCG	ENSP00000360605.4:p.Ser593=
ENST00000371553.7:c.1842_1843delinsCG	ENSP00000360608.3:p.Ser614=
ENST00000371555.8:c.1842_1843delinsCG	ENSP00000360610.4:p.Ser614=
ENST00000371559.8:c.1779_1780delinsCG	ENSP00000360614.4:p.Ser593=
ENST00000371560.4:c.1842_1843delinsCG	ENSP00000360615.3:p.Ser614=
ENST00000371561.7:c.1779_1780delinsCG	ENSP00000360616.3:p.Ser593=
ENST00000471122.5:n.1856_1857delinsCG
NM_000832.6:c.1779_1780delinsCG	NP_000823.4:p.Ser593=
NM_001185090.1:c.1842_1843delinsCG	NP_001172019.1:p.Ser614=
NM_001185091.1:c.1842_1843delinsCG	NP_001172020.1:p.Ser614=
NM_007327.3:c.1779_1780delinsCG	NP_015566.1:p.Ser593=
NM_021569.3:c.1779_1780delinsCG	NP_067544.1:p.Ser593=
XM_005266071.2:c.1779_1780delinsCG	XP_005266128.1:p.Ser593=
XM_005266072.2:c.1842_1843delinsCG	XP_005266129.1:p.Ser614=
XM_005266073.3:c.1842_1843delinsCG	XP_005266130.1:p.Ser614=
XM_011518583.1:c.1842_1843delinsCG	XP_011516885.1:p.Ser614=
XM_005266071.3:c.1779_1780delinsCG	XP_005266128.1:p.Ser593=
XM_005266072.3:c.1842_1843delinsCG	XP_005266129.1:p.Ser614=
XM_005266073.4:c.1842_1843delinsCG	XP_005266130.1:p.Ser614=
XM_011518583.2:c.1842_1843delinsCG	XP_011516885.1:p.Ser614=
NM_007327.4:c.1779_1780delinsCG MANE Select	NP_015566.1:p.Ser593=
NM_000832.7:c.1779_1780delinsCG	NP_000823.4:p.Ser593=
NM_001185090.2:c.1842_1843delinsCG	NP_001172019.1:p.Ser614=
NM_001185091.2:c.1842_1843delinsCG	NP_001172020.1:p.Ser614=
NM_021569.4:c.1779_1780delinsCG	NP_067544.1:p.Ser593=