Canonical Allele Identifier: CA467790107

Gene: GRIN1

Linked Data

• MyVariant Identifiers: chr9:g.140053081T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137158629T>C , CM000671.2:g.137158629T>C	GRCh38
NC_000009.11:g.140053081T>C , CM000671.1:g.140053081T>C	GRCh37
NC_000009.10:g.139172902T>C	NCBI36
NG_011507.1:g.24473T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371553.8:c.1185T>C	ENSP00000360608.3:p.Pro395=
ENST00000371560.5:c.1185T>C	ENSP00000360615.3:p.Pro395=
ENST00000371561.8:c.1122T>C MANE Select	ENSP00000360616.3:p.Pro374=
ENST00000675295.1:n.552T>C
ENST00000676396.1:n.2632T>C
ENST00000350902.9:c.*97T>C	ENSP00000316915.9:n.*97T>C
ENST00000371546.8:c.1185T>C	ENSP00000360601.4:p.Pro395=
ENST00000371550.8:c.1122T>C	ENSP00000360605.4:p.Pro374=
ENST00000371553.7:c.1185T>C	ENSP00000360608.3:p.Pro395=
ENST00000371555.8:c.1185T>C	ENSP00000360610.4:p.Pro395=
ENST00000371559.8:c.1122T>C	ENSP00000360614.4:p.Pro374=
ENST00000371560.4:c.1185T>C	ENSP00000360615.3:p.Pro395=
ENST00000371561.7:c.1122T>C	ENSP00000360616.3:p.Pro374=
ENST00000471122.5:n.1199T>C
ENST00000485413.1:n.313T>C
NM_000832.6:c.1122T>C	NP_000823.4:p.Pro374=
NM_001185090.1:c.1185T>C	NP_001172019.1:p.Pro395=
NM_001185091.1:c.1185T>C	NP_001172020.1:p.Pro395=
NM_007327.3:c.1122T>C	NP_015566.1:p.Pro374=
NM_021569.3:c.1122T>C	NP_067544.1:p.Pro374=
XM_005266071.2:c.1122T>C	XP_005266128.1:p.Pro374=
XM_005266072.2:c.1185T>C	XP_005266129.1:p.Pro395=
XM_005266073.3:c.1185T>C	XP_005266130.1:p.Pro395=
XM_011518583.1:c.1185T>C	XP_011516885.1:p.Pro395=
XM_005266071.3:c.1122T>C	XP_005266128.1:p.Pro374=
XM_005266072.3:c.1185T>C	XP_005266129.1:p.Pro395=
XM_005266073.4:c.1185T>C	XP_005266130.1:p.Pro395=
XM_011518583.2:c.1185T>C	XP_011516885.1:p.Pro395=
NM_007327.4:c.1122T>C MANE Select	NP_015566.1:p.Pro374=
NM_000832.7:c.1122T>C	NP_000823.4:p.Pro374=
NM_001185090.2:c.1185T>C	NP_001172019.1:p.Pro395=
NM_001185091.2:c.1185T>C	NP_001172020.1:p.Pro395=
NM_021569.4:c.1122T>C	NP_067544.1:p.Pro374=