Canonical Allele Identifier: CA5360792

Gene: GRIN1

Linked Data

• dbSNP Id: rs769967011
• ExAC: 9:140051511 CTGGGCGGGGCTGCTCTTGGGGAGG / C
• gnomAD v2: 9-140051511-CTGGGCGGGGCTGCTCTTGGGGAGG-C
• gnomAD v4: 9-137157059-CTGGGCGGGGCTGCTCTTGGGGAGG-C
• MyVariant Identifiers: chr9:g.140051512_140051535del (hg19) ; chr9:g.140051521_140051556delinsTCACTCCAGAGA (hg19) ; chr9:g.137157060_137157083del (hg38) ; chr9:g.137157069_137157104delinsTCACTCCAGAGA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137157069_137157092del , CM000671.2:g.137157069_137157092del	GRCh38
NC_000009.11:g.140051521_140051544del , CM000671.1:g.140051521_140051544del	GRCh37
NC_000009.10:g.139171342_139171365del	NCBI36
NG_011507.1:g.22913_22936del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371553.8:c.1031+32_1031+55del	ENSP00000360608.3:n.1031+32_1031+55del
ENST00000371560.5:c.1031+32_1031+55del	ENSP00000360615.3:n.1031+32_1031+55del
ENST00000371561.8:c.968+32_968+55del MANE Select	ENSP00000360616.3:n.968+32_968+55del
ENST00000675295.1:n.398+32_398+55del
ENST00000676396.1:n.2478+32_2478+55del
ENST00000350902.9:c.1014+32_1014+55del	ENSP00000316915.9:n.1014+32_1014+55del
ENST00000371546.8:c.1031+32_1031+55del	ENSP00000360601.4:n.1031+32_1031+55del
ENST00000371550.8:c.968+32_968+55del	ENSP00000360605.4:n.968+32_968+55del
ENST00000371553.7:c.1031+32_1031+55del	ENSP00000360608.3:n.1031+32_1031+55del
ENST00000371555.8:c.1031+32_1031+55del	ENSP00000360610.4:n.1031+32_1031+55del
ENST00000371559.8:c.968+32_968+55del	ENSP00000360614.4:n.968+32_968+55del
ENST00000371560.4:c.1031+32_1031+55del	ENSP00000360615.3:n.1031+32_1031+55del
ENST00000371561.7:c.968+32_968+55del	ENSP00000360616.3:n.968+32_968+55del
ENST00000471122.5:n.1045+32_1045+55del
ENST00000485413.1:n.62+32_62+55del
NM_000832.6:c.968+32_968+55del	NP_000823.4:n.968+32_968+55del
NM_001185090.1:c.1031+32_1031+55del	NP_001172019.1:n.1031+32_1031+55del
NM_001185091.1:c.1031+32_1031+55del	NP_001172020.1:n.1031+32_1031+55del
NM_007327.3:c.968+32_968+55del	NP_015566.1:n.968+32_968+55del
NM_021569.3:c.968+32_968+55del	NP_067544.1:n.968+32_968+55del
XM_005266071.2:c.968+32_968+55del	XP_005266128.1:n.968+32_968+55del
XM_005266072.2:c.1031+32_1031+55del	XP_005266129.1:n.1031+32_1031+55del
XM_005266073.3:c.1031+32_1031+55del	XP_005266130.1:n.1031+32_1031+55del
XM_011518583.1:c.1031+32_1031+55del	XP_011516885.1:n.1031+32_1031+55del
XM_005266071.3:c.968+32_968+55del	XP_005266128.1:n.968+32_968+55del
XM_005266072.3:c.1031+32_1031+55del	XP_005266129.1:n.1031+32_1031+55del
XM_005266073.4:c.1031+32_1031+55del	XP_005266130.1:n.1031+32_1031+55del
XM_011518583.2:c.1031+32_1031+55del	XP_011516885.1:n.1031+32_1031+55del
NM_007327.4:c.968+32_968+55del MANE Select	NP_015566.1:n.968+32_968+55del
NM_000832.7:c.968+32_968+55del	NP_000823.4:n.968+32_968+55del
NM_001185090.2:c.1031+32_1031+55del	NP_001172019.1:n.1031+32_1031+55del
NM_001185091.2:c.1031+32_1031+55del	NP_001172020.1:n.1031+32_1031+55del
NM_021569.4:c.968+32_968+55del	NP_067544.1:n.968+32_968+55del