Canonical Allele Identifier: CA375720763

Gene: GRIN1

Linked Data

• ClinVar Variation Id: 917873
• ClinVar RCV Id: RCV001175148 ; RCV002293250
• dbSNP Id: rs1833621434
• MyVariant Identifiers: chr9:g.140057111G>T (hg19) ; chr9:g.137162659G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137162659G>T , CM000671.2:g.137162659G>T	GRCh38
NC_000009.11:g.140057111G>T , CM000671.1:g.140057111G>T	GRCh37
NC_000009.10:g.139176932G>T	NCBI36
NG_011507.1:g.28503G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371553.8:c.1996G>T	ENSP00000360608.3:p.Ala666Ser
ENST00000371560.5:c.1996G>T	ENSP00000360615.3:p.Ala666Ser
ENST00000371561.8:c.1933G>T MANE Select	ENSP00000360616.3:p.Ala645Ser
ENST00000675295.1:n.1363G>T
ENST00000350902.9:c.*908G>T	ENSP00000316915.9:n.*908G>T
ENST00000371546.8:c.1996G>T	ENSP00000360601.4:p.Ala666Ser
ENST00000371550.8:c.1933G>T	ENSP00000360605.4:p.Ala645Ser
ENST00000371553.7:c.1996G>T	ENSP00000360608.3:p.Ala666Ser
ENST00000371555.8:c.1996G>T	ENSP00000360610.4:p.Ala666Ser
ENST00000371559.8:c.1933G>T	ENSP00000360614.4:p.Ala645Ser
ENST00000371560.4:c.1996G>T	ENSP00000360615.3:p.Ala666Ser
ENST00000371561.7:c.1933G>T	ENSP00000360616.3:p.Ala645Ser
ENST00000471122.5:n.2010G>T
NM_000832.6:c.1933G>T	NP_000823.4:p.Ala645Ser
NM_001185090.1:c.1996G>T	NP_001172019.1:p.Ala666Ser
NM_001185091.1:c.1996G>T	NP_001172020.1:p.Ala666Ser
NM_007327.3:c.1933G>T	NP_015566.1:p.Ala645Ser
NM_021569.3:c.1933G>T	NP_067544.1:p.Ala645Ser
XM_005266071.2:c.1933G>T	XP_005266128.1:p.Ala645Ser
XM_005266072.2:c.1996G>T	XP_005266129.1:p.Ala666Ser
XM_005266073.3:c.1996G>T	XP_005266130.1:p.Ala666Ser
XM_011518583.1:c.1996G>T	XP_011516885.1:p.Ala666Ser
XM_005266071.3:c.1933G>T	XP_005266128.1:p.Ala645Ser
XM_005266072.3:c.1996G>T	XP_005266129.1:p.Ala666Ser
XM_005266073.4:c.1996G>T	XP_005266130.1:p.Ala666Ser
XM_011518583.2:c.1996G>T	XP_011516885.1:p.Ala666Ser
NM_007327.4:c.1933G>T MANE Select	NP_015566.1:p.Ala645Ser
NM_000832.7:c.1933G>T	NP_000823.4:p.Ala645Ser
NM_001185090.2:c.1996G>T	NP_001172019.1:p.Ala666Ser
NM_001185091.2:c.1996G>T	NP_001172020.1:p.Ala666Ser
NM_021569.4:c.1933G>T	NP_067544.1:p.Ala645Ser