Canonical Allele Identifier: CA375714658

Gene: GRIN1

Linked Data

• MyVariant Identifiers: chr9:g.140051141T>C (hg19) ; chr9:g.137156689T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137156689T>C , CM000671.2:g.137156689T>C	GRCh38
NC_000009.11:g.140051141T>C , CM000671.1:g.140051141T>C	GRCh37
NC_000009.10:g.139170962T>C	NCBI36
NG_011507.1:g.22533T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371553.8:c.755T>C	ENSP00000360608.3:p.Val252Ala
ENST00000371560.5:c.755T>C	ENSP00000360615.3:p.Val252Ala
ENST00000371561.8:c.692T>C MANE Select	ENSP00000360616.3:p.Val231Ala
ENST00000675295.1:n.122T>C
ENST00000676396.1:n.2202T>C
ENST00000350902.9:c.755T>C	ENSP00000316915.9:p.Val252Ala
ENST00000371546.8:c.755T>C	ENSP00000360601.4:p.Val252Ala
ENST00000371550.8:c.692T>C	ENSP00000360605.4:p.Val231Ala
ENST00000371553.7:c.755T>C	ENSP00000360608.3:p.Val252Ala
ENST00000371555.8:c.755T>C	ENSP00000360610.4:p.Val252Ala
ENST00000371559.8:c.692T>C	ENSP00000360614.4:p.Val231Ala
ENST00000371560.4:c.755T>C	ENSP00000360615.3:p.Val252Ala
ENST00000371561.7:c.692T>C	ENSP00000360616.3:p.Val231Ala
ENST00000471122.5:n.769T>C
NM_000832.6:c.692T>C	NP_000823.4:p.Val231Ala
NM_001185090.1:c.755T>C	NP_001172019.1:p.Val252Ala
NM_001185091.1:c.755T>C	NP_001172020.1:p.Val252Ala
NM_007327.3:c.692T>C	NP_015566.1:p.Val231Ala
NM_021569.3:c.692T>C	NP_067544.1:p.Val231Ala
XM_005266071.2:c.692T>C	XP_005266128.1:p.Val231Ala
XM_005266072.2:c.755T>C	XP_005266129.1:p.Val252Ala
XM_005266073.3:c.755T>C	XP_005266130.1:p.Val252Ala
XM_011518583.1:c.755T>C	XP_011516885.1:p.Val252Ala
XM_005266071.3:c.692T>C	XP_005266128.1:p.Val231Ala
XM_005266072.3:c.755T>C	XP_005266129.1:p.Val252Ala
XM_005266073.4:c.755T>C	XP_005266130.1:p.Val252Ala
XM_011518583.2:c.755T>C	XP_011516885.1:p.Val252Ala
NM_007327.4:c.692T>C MANE Select	NP_015566.1:p.Val231Ala
NM_000832.7:c.692T>C	NP_000823.4:p.Val231Ala
NM_001185090.2:c.755T>C	NP_001172019.1:p.Val252Ala
NM_001185091.2:c.755T>C	NP_001172020.1:p.Val252Ala
NM_021569.4:c.692T>C	NP_067544.1:p.Val231Ala