Canonical Allele Identifier: CA375714917

Gene: GRIN1

Linked Data

• MyVariant Identifiers: chr9:g.140051330A>T (hg19) ; chr9:g.137156878A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137156878A>T , CM000671.2:g.137156878A>T	GRCh38
NC_000009.11:g.140051330A>T , CM000671.1:g.140051330A>T	GRCh37
NC_000009.10:g.139171151A>T	NCBI36
NG_011507.1:g.22722A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371553.8:c.872A>T	ENSP00000360608.3:p.Gln291Leu
ENST00000371560.5:c.872A>T	ENSP00000360615.3:p.Gln291Leu
ENST00000371561.8:c.809A>T MANE Select	ENSP00000360616.3:p.Gln270Leu
ENST00000675295.1:n.239A>T
ENST00000676396.1:n.2319A>T
ENST00000350902.9:c.857-2A>T	ENSP00000316915.9:n.857-2A>T
ENST00000371546.8:c.872A>T	ENSP00000360601.4:p.Gln291Leu
ENST00000371550.8:c.809A>T	ENSP00000360605.4:p.Gln270Leu
ENST00000371553.7:c.872A>T	ENSP00000360608.3:p.Gln291Leu
ENST00000371555.8:c.872A>T	ENSP00000360610.4:p.Gln291Leu
ENST00000371559.8:c.809A>T	ENSP00000360614.4:p.Gln270Leu
ENST00000371560.4:c.872A>T	ENSP00000360615.3:p.Gln291Leu
ENST00000371561.7:c.809A>T	ENSP00000360616.3:p.Gln270Leu
ENST00000471122.5:n.886A>T
NM_000832.6:c.809A>T	NP_000823.4:p.Gln270Leu
NM_001185090.1:c.872A>T	NP_001172019.1:p.Gln291Leu
NM_001185091.1:c.872A>T	NP_001172020.1:p.Gln291Leu
NM_007327.3:c.809A>T	NP_015566.1:p.Gln270Leu
NM_021569.3:c.809A>T	NP_067544.1:p.Gln270Leu
XM_005266071.2:c.809A>T	XP_005266128.1:p.Gln270Leu
XM_005266072.2:c.872A>T	XP_005266129.1:p.Gln291Leu
XM_005266073.3:c.872A>T	XP_005266130.1:p.Gln291Leu
XM_011518583.1:c.872A>T	XP_011516885.1:p.Gln291Leu
XM_005266071.3:c.809A>T	XP_005266128.1:p.Gln270Leu
XM_005266072.3:c.872A>T	XP_005266129.1:p.Gln291Leu
XM_005266073.4:c.872A>T	XP_005266130.1:p.Gln291Leu
XM_011518583.2:c.872A>T	XP_011516885.1:p.Gln291Leu
NM_007327.4:c.809A>T MANE Select	NP_015566.1:p.Gln270Leu
NM_000832.7:c.809A>T	NP_000823.4:p.Gln270Leu
NM_001185090.2:c.872A>T	NP_001172019.1:p.Gln291Leu
NM_001185091.2:c.872A>T	NP_001172020.1:p.Gln291Leu
NM_021569.4:c.809A>T	NP_067544.1:p.Gln270Leu