Canonical Allele Identifier: CA467850586

Gene: GRIN1

Linked Data

• gnomAD v4: 9-137156780-C-T
• COSMIC: COSM6359479 ; COSM6359480
• MyVariant Identifiers: chr9:g.140051232C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137156780C>T , CM000671.2:g.137156780C>T	GRCh38
NC_000009.11:g.140051232C>T , CM000671.1:g.140051232C>T	GRCh37
NC_000009.10:g.139171053C>T	NCBI36
NG_011507.1:g.22624C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371553.8:c.846C>T	ENSP00000360608.3:p.Tyr282=
ENST00000371560.5:c.846C>T	ENSP00000360615.3:p.Tyr282=
ENST00000371561.8:c.783C>T MANE Select	ENSP00000360616.3:p.Tyr261=
ENST00000675295.1:n.213C>T
ENST00000676396.1:n.2293C>T
ENST00000350902.9:c.846C>T	ENSP00000316915.9:p.Tyr282=
ENST00000371546.8:c.846C>T	ENSP00000360601.4:p.Tyr282=
ENST00000371550.8:c.783C>T	ENSP00000360605.4:p.Tyr261=
ENST00000371553.7:c.846C>T	ENSP00000360608.3:p.Tyr282=
ENST00000371555.8:c.846C>T	ENSP00000360610.4:p.Tyr282=
ENST00000371559.8:c.783C>T	ENSP00000360614.4:p.Tyr261=
ENST00000371560.4:c.846C>T	ENSP00000360615.3:p.Tyr282=
ENST00000371561.7:c.783C>T	ENSP00000360616.3:p.Tyr261=
ENST00000471122.5:n.860C>T
NM_000832.6:c.783C>T	NP_000823.4:p.Tyr261=
NM_001185090.1:c.846C>T	NP_001172019.1:p.Tyr282=
NM_001185091.1:c.846C>T	NP_001172020.1:p.Tyr282=
NM_007327.3:c.783C>T	NP_015566.1:p.Tyr261=
NM_021569.3:c.783C>T	NP_067544.1:p.Tyr261=
XM_005266071.2:c.783C>T	XP_005266128.1:p.Tyr261=
XM_005266072.2:c.846C>T	XP_005266129.1:p.Tyr282=
XM_005266073.3:c.846C>T	XP_005266130.1:p.Tyr282=
XM_011518583.1:c.846C>T	XP_011516885.1:p.Tyr282=
XM_005266071.3:c.783C>T	XP_005266128.1:p.Tyr261=
XM_005266072.3:c.846C>T	XP_005266129.1:p.Tyr282=
XM_005266073.4:c.846C>T	XP_005266130.1:p.Tyr282=
XM_011518583.2:c.846C>T	XP_011516885.1:p.Tyr282=
NM_007327.4:c.783C>T MANE Select	NP_015566.1:p.Tyr261=
NM_000832.7:c.783C>T	NP_000823.4:p.Tyr261=
NM_001185090.2:c.846C>T	NP_001172019.1:p.Tyr282=
NM_001185091.2:c.846C>T	NP_001172020.1:p.Tyr282=
NM_021569.4:c.783C>T	NP_067544.1:p.Tyr261=