Canonical Allele Identifier: CA467788400

Gene: GRIN1

Linked Data

• MyVariant Identifiers: chr9:g.140033980C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137139528C>G , CM000671.2:g.137139528C>G	GRCh38
NC_000009.11:g.140033980C>G , CM000671.1:g.140033980C>G	GRCh37
NC_000009.10:g.139153801C>G	NCBI36
NG_011507.1:g.5372C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371553.8:c.42C>G	ENSP00000360608.3:p.Ser14=
ENST00000371560.5:c.42C>G	ENSP00000360615.3:p.Ser14=
ENST00000371561.8:c.42C>G MANE Select	ENSP00000360616.3:p.Ser14=
ENST00000350902.9:c.42C>G	ENSP00000316915.9:p.Ser14=
ENST00000371546.8:c.42C>G	ENSP00000360601.4:p.Ser14=
ENST00000371550.8:c.42C>G	ENSP00000360605.4:p.Ser14=
ENST00000371553.7:c.42C>G	ENSP00000360608.3:p.Ser14=
ENST00000371555.8:c.42C>G	ENSP00000360610.4:p.Ser14=
ENST00000371559.8:c.42C>G	ENSP00000360614.4:p.Ser14=
ENST00000371560.4:c.42C>G	ENSP00000360615.3:p.Ser14=
ENST00000371561.7:c.42C>G	ENSP00000360616.3:p.Ser14=
ENST00000471122.5:n.119C>G
NM_000832.6:c.42C>G	NP_000823.4:p.Ser14=
NM_001185090.1:c.42C>G	NP_001172019.1:p.Ser14=
NM_001185091.1:c.42C>G	NP_001172020.1:p.Ser14=
NM_007327.3:c.42C>G	NP_015566.1:p.Ser14=
NM_021569.3:c.42C>G	NP_067544.1:p.Ser14=
XM_005266071.2:c.42C>G	XP_005266128.1:p.Ser14=
XM_005266072.2:c.42C>G	XP_005266129.1:p.Ser14=
XM_005266073.3:c.42C>G	XP_005266130.1:p.Ser14=
XM_011518583.1:c.42C>G	XP_011516885.1:p.Ser14=
XM_005266071.3:c.42C>G	XP_005266128.1:p.Ser14=
XM_005266072.3:c.42C>G	XP_005266129.1:p.Ser14=
XM_005266073.4:c.42C>G	XP_005266130.1:p.Ser14=
XM_011518583.2:c.42C>G	XP_011516885.1:p.Ser14=
NM_007327.4:c.42C>G MANE Select	NP_015566.1:p.Ser14=
NM_000832.7:c.42C>G	NP_000823.4:p.Ser14=
NM_001185090.2:c.42C>G	NP_001172019.1:p.Ser14=
NM_001185091.2:c.42C>G	NP_001172020.1:p.Ser14=
NM_021569.4:c.42C>G	NP_067544.1:p.Ser14=