Canonical Allele Identifier: CA1884318386

Gene: GRIN1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137139447G= , CM000671.2:g.137139447G=	GRCh38
NC_000009.11:g.140033899G= , CM000671.1:g.140033899G=	GRCh37
NC_000009.10:g.139153720G=	NCBI36
NG_011507.1:g.5291G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371553.8:c.-40G=	ENSP00000360608.3:n.-40G=
ENST00000371560.5:c.-40G=	ENSP00000360615.3:n.-40G=
ENST00000371561.8:c.-40G= MANE Select	ENSP00000360616.3:n.-40G=
ENST00000350902.9:c.-40G=	ENSP00000316915.9:n.-40G=
ENST00000371561.7:c.-40G=	ENSP00000360616.3:n.-40G=
ENST00000471122.5:n.38G=
NM_000832.6:c.-40G=	NP_000823.4:n.-40G=
NM_001185090.1:c.-40G=	NP_001172019.1:n.-40G=
NM_001185091.1:c.-40G=	NP_001172020.1:n.-40G=
NM_007327.3:c.-40G=	NP_015566.1:n.-40G=
NM_021569.3:c.-40G=	NP_067544.1:n.-40G=
XM_005266071.2:c.-40G=	XP_005266128.1:n.-40G=
XM_005266072.2:c.-40G=	XP_005266129.1:n.-40G=
XM_005266073.3:c.-40G=	XP_005266130.1:n.-40G=
XM_011518583.1:c.-40G=	XP_011516885.1:n.-40G=
XM_005266072.3:c.-40G=	XP_005266129.1:n.-40G=
XM_005266073.4:c.-40G=	XP_005266130.1:n.-40G=
XM_011518583.2:c.-40G=	XP_011516885.1:n.-40G=
NM_007327.4:c.-40G= MANE Select	NP_015566.1:n.-40G=
NM_000832.7:c.-40G=	NP_000823.4:n.-40G=
NM_001185090.2:c.-40G=	NP_001172019.1:n.-40G=
NM_001185091.2:c.-40G=	NP_001172020.1:n.-40G=
NM_021569.4:c.-40G=	NP_067544.1:n.-40G=