Canonical Allele Identifier: CA1884328244

Gene: GRIN1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137157121_137157122delinsTG , CM000671.2:g.137157121_137157122delinsTG	GRCh38
NC_000009.11:g.140051573_140051574delinsTG , CM000671.1:g.140051573_140051574delinsTG	GRCh37
NC_000009.10:g.139171394_139171395delinsTG	NCBI36
NG_011507.1:g.22965_22966delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371553.8:c.1031+84_1031+85delinsTG	ENSP00000360608.3:n.1031+84_1031+85delinsTG
ENST00000371560.5:c.1031+84_1031+85delinsTG	ENSP00000360615.3:n.1031+84_1031+85delinsTG
ENST00000371561.8:c.968+84_968+85delinsTG MANE Select	ENSP00000360616.3:n.968+84_968+85delinsTG
ENST00000675295.1:n.398+84_398+85delinsTG
ENST00000676396.1:n.2478+84_2478+85delinsTG
ENST00000350902.9:c.1014+84_1014+85delinsTG	ENSP00000316915.9:n.1014+84_1014+85delinsTG
ENST00000371546.8:c.1031+84_1031+85delinsTG	ENSP00000360601.4:n.1031+84_1031+85delinsTG
ENST00000371550.8:c.968+84_968+85delinsTG	ENSP00000360605.4:n.968+84_968+85delinsTG
ENST00000371553.7:c.1031+84_1031+85delinsTG	ENSP00000360608.3:n.1031+84_1031+85delinsTG
ENST00000371555.8:c.1031+84_1031+85delinsTG	ENSP00000360610.4:n.1031+84_1031+85delinsTG
ENST00000371559.8:c.968+84_968+85delinsTG	ENSP00000360614.4:n.968+84_968+85delinsTG
ENST00000371560.4:c.1031+84_1031+85delinsTG	ENSP00000360615.3:n.1031+84_1031+85delinsTG
ENST00000371561.7:c.968+84_968+85delinsTG	ENSP00000360616.3:n.968+84_968+85delinsTG
ENST00000471122.5:n.1045+84_1045+85delinsTG
ENST00000485413.1:n.62+84_62+85delinsTG
NM_000832.6:c.968+84_968+85delinsTG	NP_000823.4:n.968+84_968+85delinsTG
NM_001185090.1:c.1031+84_1031+85delinsTG	NP_001172019.1:n.1031+84_1031+85delinsTG
NM_001185091.1:c.1031+84_1031+85delinsTG	NP_001172020.1:n.1031+84_1031+85delinsTG
NM_007327.3:c.968+84_968+85delinsTG	NP_015566.1:n.968+84_968+85delinsTG
NM_021569.3:c.968+84_968+85delinsTG	NP_067544.1:n.968+84_968+85delinsTG
XM_005266071.2:c.968+84_968+85delinsTG	XP_005266128.1:n.968+84_968+85delinsTG
XM_005266072.2:c.1031+84_1031+85delinsTG	XP_005266129.1:n.1031+84_1031+85delinsTG
XM_005266073.3:c.1031+84_1031+85delinsTG	XP_005266130.1:n.1031+84_1031+85delinsTG
XM_011518583.1:c.1031+84_1031+85delinsTG	XP_011516885.1:n.1031+84_1031+85delinsTG
XM_005266071.3:c.968+84_968+85delinsTG	XP_005266128.1:n.968+84_968+85delinsTG
XM_005266072.3:c.1031+84_1031+85delinsTG	XP_005266129.1:n.1031+84_1031+85delinsTG
XM_005266073.4:c.1031+84_1031+85delinsTG	XP_005266130.1:n.1031+84_1031+85delinsTG
XM_011518583.2:c.1031+84_1031+85delinsTG	XP_011516885.1:n.1031+84_1031+85delinsTG
NM_007327.4:c.968+84_968+85delinsTG MANE Select	NP_015566.1:n.968+84_968+85delinsTG
NM_000832.7:c.968+84_968+85delinsTG	NP_000823.4:n.968+84_968+85delinsTG
NM_001185090.2:c.1031+84_1031+85delinsTG	NP_001172019.1:n.1031+84_1031+85delinsTG
NM_001185091.2:c.1031+84_1031+85delinsTG	NP_001172020.1:n.1031+84_1031+85delinsTG
NM_021569.4:c.968+84_968+85delinsTG	NP_067544.1:n.968+84_968+85delinsTG