Canonical Allele Identifier: CA1884328884

Gene: GRIN1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137158421C= , CM000671.2:g.137158421C=	GRCh38
NC_000009.11:g.140052873C= , CM000671.1:g.140052873C=	GRCh37
NC_000009.10:g.139172694C=	NCBI36
NG_011507.1:g.24265C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000371553.8:c.1074C=	ENSP00000360608.3:p.Arg358=
ENST00000371560.5:c.1074C=	ENSP00000360615.3:p.Arg358=
ENST00000371561.8:c.1011C= MANE Select	ENSP00000360616.3:p.Arg337=
ENST00000675295.1:n.441C=
ENST00000676396.1:n.2521C=
ENST00000350902.9:c.1057C=	ENSP00000316915.9:p.Arg353=
ENST00000371546.8:c.1074C=	ENSP00000360601.4:p.Arg358=
ENST00000371550.8:c.1011C=	ENSP00000360605.4:p.Arg337=
ENST00000371553.7:c.1074C=	ENSP00000360608.3:p.Arg358=
ENST00000371555.8:c.1074C=	ENSP00000360610.4:p.Arg358=
ENST00000371559.8:c.1011C=	ENSP00000360614.4:p.Arg337=
ENST00000371560.4:c.1074C=	ENSP00000360615.3:p.Arg358=
ENST00000371561.7:c.1011C=	ENSP00000360616.3:p.Arg337=
ENST00000471122.5:n.1088C=
ENST00000485413.1:n.105C=
NM_000832.6:c.1011C=	NP_000823.4:p.Arg337=
NM_001185090.1:c.1074C=	NP_001172019.1:p.Arg358=
NM_001185091.1:c.1074C=	NP_001172020.1:p.Arg358=
NM_007327.3:c.1011C=	NP_015566.1:p.Arg337=
NM_021569.3:c.1011C=	NP_067544.1:p.Arg337=
XM_005266071.2:c.1011C=	XP_005266128.1:p.Arg337=
XM_005266072.2:c.1074C=	XP_005266129.1:p.Arg358=
XM_005266073.3:c.1074C=	XP_005266130.1:p.Arg358=
XM_011518583.1:c.1074C=	XP_011516885.1:p.Arg358=
XM_005266071.3:c.1011C=	XP_005266128.1:p.Arg337=
XM_005266072.3:c.1074C=	XP_005266129.1:p.Arg358=
XM_005266073.4:c.1074C=	XP_005266130.1:p.Arg358=
XM_011518583.2:c.1074C=	XP_011516885.1:p.Arg358=
NM_007327.4:c.1011C= MANE Select	NP_015566.1:p.Arg337=
NM_000832.7:c.1011C=	NP_000823.4:p.Arg337=
NM_001185090.2:c.1074C=	NP_001172019.1:p.Arg358=
NM_001185091.2:c.1074C=	NP_001172020.1:p.Arg358=
NM_021569.4:c.1011C=	NP_067544.1:p.Arg337=