Canonical Allele Identifier: CA375729542

Gene: GRIN1

Linked Data

• ClinVar Variation Id: 1702541
• ClinVar RCV Id: RCV002278859
• dbSNP Id: rs2131314853
• MyVariant Identifiers: chr9:g.140061867C>G (hg19) ; chr9:g.137167415C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137167415C>G , CM000671.2:g.137167415C>G	GRCh38
NC_000009.11:g.140061867C>G , CM000671.1:g.140061867C>G	GRCh37
NC_000009.10:g.139181688C>G	NCBI36
NG_011507.1:g.33259C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000371553.8:c.2764-359C>G	ENSP00000360608.3:n.2764-359C>G
ENST00000371560.5:c.2653-359C>G	ENSP00000360615.3:n.2653-359C>G
ENST00000371561.8:c.2705C>G MANE Select	ENSP00000360616.3:p.Thr902Ser
ENST00000371546.8:c.2768C>G	ENSP00000360601.4:p.Thr923Ser
ENST00000371550.8:c.2594C>G	ENSP00000360605.4:p.Thr865Ser
ENST00000371553.7:c.2764-359C>G	ENSP00000360608.3:n.2764-359C>G
ENST00000371555.8:c.2657C>G	ENSP00000360610.4:p.Thr886Ser
ENST00000371559.8:c.2590-359C>G	ENSP00000360614.4:n.2590-359C>G
ENST00000371560.4:c.2653-359C>G	ENSP00000360615.3:n.2653-359C>G
ENST00000371561.7:c.2705C>G	ENSP00000360616.3:p.Thr902Ser
ENST00000473811.1:n.185C>G
NM_000832.6:c.2590-359C>G	NP_000823.4:n.2590-359C>G
NM_001185090.1:c.2764-359C>G	NP_001172019.1:n.2764-359C>G
NM_001185091.1:c.2653-359C>G	NP_001172020.1:n.2653-359C>G
NM_007327.3:c.2705C>G	NP_015566.1:p.Thr902Ser
NM_021569.3:c.2594C>G	NP_067544.1:p.Thr865Ser
XM_005266071.2:c.2701-359C>G	XP_005266128.1:n.2701-359C>G
XM_005266072.2:c.2657C>G	XP_005266129.1:p.Thr886Ser
XM_005266073.3:c.2768C>G	XP_005266130.1:p.Thr923Ser
XM_005266071.3:c.2701-359C>G	XP_005266128.1:n.2701-359C>G
XM_005266072.3:c.2657C>G	XP_005266129.1:p.Thr886Ser
XM_005266073.4:c.2768C>G	XP_005266130.1:p.Thr923Ser
NM_007327.4:c.2705C>G MANE Select	NP_015566.1:p.Thr902Ser
NM_000832.7:c.2590-359C>G	NP_000823.4:n.2590-359C>G
NM_001185090.2:c.2764-359C>G	NP_001172019.1:n.2764-359C>G
NM_001185091.2:c.2653-359C>G	NP_001172020.1:n.2653-359C>G
NM_021569.4:c.2594C>G	NP_067544.1:p.Thr865Ser