Canonical Allele Identifier: CA467850981

Gene: GRIN1

Linked Data

• dbSNP Id: rs1833264662
• MyVariant Identifiers: chr9:g.140051436G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137156984G>A , CM000671.2:g.137156984G>A	GRCh38
NC_000009.11:g.140051436G>A , CM000671.1:g.140051436G>A	GRCh37
NC_000009.10:g.139171257G>A	NCBI36
NG_011507.1:g.22828G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371553.8:c.978G>A	ENSP00000360608.3:p.Pro326=
ENST00000371560.5:c.978G>A	ENSP00000360615.3:p.Pro326=
ENST00000371561.8:c.915G>A MANE Select	ENSP00000360616.3:p.Pro305=
ENST00000675295.1:n.345G>A
ENST00000676396.1:n.2425G>A
ENST00000350902.9:c.961G>A	ENSP00000316915.9:p.Ala321Thr
ENST00000371546.8:c.978G>A	ENSP00000360601.4:p.Pro326=
ENST00000371550.8:c.915G>A	ENSP00000360605.4:p.Pro305=
ENST00000371553.7:c.978G>A	ENSP00000360608.3:p.Pro326=
ENST00000371555.8:c.978G>A	ENSP00000360610.4:p.Pro326=
ENST00000371559.8:c.915G>A	ENSP00000360614.4:p.Pro305=
ENST00000371560.4:c.978G>A	ENSP00000360615.3:p.Pro326=
ENST00000371561.7:c.915G>A	ENSP00000360616.3:p.Pro305=
ENST00000471122.5:n.992G>A
ENST00000485413.1:n.9G>A
NM_000832.6:c.915G>A	NP_000823.4:p.Pro305=
NM_001185090.1:c.978G>A	NP_001172019.1:p.Pro326=
NM_001185091.1:c.978G>A	NP_001172020.1:p.Pro326=
NM_007327.3:c.915G>A	NP_015566.1:p.Pro305=
NM_021569.3:c.915G>A	NP_067544.1:p.Pro305=
XM_005266071.2:c.915G>A	XP_005266128.1:p.Pro305=
XM_005266072.2:c.978G>A	XP_005266129.1:p.Pro326=
XM_005266073.3:c.978G>A	XP_005266130.1:p.Pro326=
XM_011518583.1:c.978G>A	XP_011516885.1:p.Pro326=
XM_005266071.3:c.915G>A	XP_005266128.1:p.Pro305=
XM_005266072.3:c.978G>A	XP_005266129.1:p.Pro326=
XM_005266073.4:c.978G>A	XP_005266130.1:p.Pro326=
XM_011518583.2:c.978G>A	XP_011516885.1:p.Pro326=
NM_007327.4:c.915G>A MANE Select	NP_015566.1:p.Pro305=
NM_000832.7:c.915G>A	NP_000823.4:p.Pro305=
NM_001185090.2:c.978G>A	NP_001172019.1:p.Pro326=
NM_001185091.2:c.978G>A	NP_001172020.1:p.Pro326=
NM_021569.4:c.915G>A	NP_067544.1:p.Pro305=