Canonical Allele Identifier: CA1884333332

Gene: GRIN1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137167458G= , CM000671.2:g.137167458G=	GRCh38
NC_000009.11:g.140061910G= , CM000671.1:g.140061910G=	GRCh37
NC_000009.10:g.139181731G=	NCBI36
NG_011507.1:g.33302G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371553.8:c.2764-316G=	ENSP00000360608.3:n.2764-316G=
ENST00000371560.5:c.2653-316G=	ENSP00000360615.3:n.2653-316G=
ENST00000371561.8:c.2748G= MANE Select	ENSP00000360616.3:p.Val916=
ENST00000371546.8:c.2811G=	ENSP00000360601.4:p.Val937=
ENST00000371550.8:c.2637G=	ENSP00000360605.4:p.Val879=
ENST00000371553.7:c.2764-316G=	ENSP00000360608.3:n.2764-316G=
ENST00000371555.8:c.2700G=	ENSP00000360610.4:p.Val900=
ENST00000371559.8:c.2590-316G=	ENSP00000360614.4:n.2590-316G=
ENST00000371560.4:c.2653-316G=	ENSP00000360615.3:n.2653-316G=
ENST00000371561.7:c.2748G=	ENSP00000360616.3:p.Val916=
ENST00000473811.1:n.228G=
NM_000832.6:c.2590-316G=	NP_000823.4:n.2590-316G=
NM_001185090.1:c.2764-316G=	NP_001172019.1:n.2764-316G=
NM_001185091.1:c.2653-316G=	NP_001172020.1:n.2653-316G=
NM_007327.3:c.2748G=	NP_015566.1:p.Val916=
NM_021569.3:c.2637G=	NP_067544.1:p.Val879=
XM_005266071.2:c.2701-316G=	XP_005266128.1:n.2701-316G=
XM_005266072.2:c.2700G=	XP_005266129.1:p.Val900=
XM_005266073.3:c.2811G=	XP_005266130.1:p.Val937=
XM_005266071.3:c.2701-316G=	XP_005266128.1:n.2701-316G=
XM_005266072.3:c.2700G=	XP_005266129.1:p.Val900=
XM_005266073.4:c.2811G=	XP_005266130.1:p.Val937=
NM_007327.4:c.2748G= MANE Select	NP_015566.1:p.Val916=
NM_000832.7:c.2590-316G=	NP_000823.4:n.2590-316G=
NM_001185090.2:c.2764-316G=	NP_001172019.1:n.2764-316G=
NM_001185091.2:c.2653-316G=	NP_001172020.1:n.2653-316G=
NM_021569.4:c.2637G=	NP_067544.1:p.Val879=