Canonical Allele Identifier: CA591372586

Gene: GRIN1

Linked Data

• dbSNP Id: rs1388977063
• gnomAD v2: 9-140051291-GCT-G
• MyVariant Identifiers: chr9:g.140051292_140051293del (hg19) ; chr9:g.137156840_137156841del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137156842_137156843del , CM000671.2:g.137156842_137156843del	GRCh38
NC_000009.11:g.140051294_140051295del , CM000671.1:g.140051294_140051295del	GRCh37
NC_000009.10:g.139171115_139171116del	NCBI36
NG_011507.1:g.22686_22687del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371553.8:c.857-21_857-20del	ENSP00000360608.3:n.857-21_857-20del
ENST00000371560.5:c.857-21_857-20del	ENSP00000360615.3:n.857-21_857-20del
ENST00000371561.8:c.794-21_794-20del MANE Select	ENSP00000360616.3:n.794-21_794-20del
ENST00000675295.1:n.224-21_224-20del
ENST00000676396.1:n.2304-21_2304-20del
ENST00000350902.9:c.857-38_857-37del	ENSP00000316915.9:n.857-38_857-37del
ENST00000371546.8:c.857-21_857-20del	ENSP00000360601.4:n.857-21_857-20del
ENST00000371550.8:c.794-21_794-20del	ENSP00000360605.4:n.794-21_794-20del
ENST00000371553.7:c.857-21_857-20del	ENSP00000360608.3:n.857-21_857-20del
ENST00000371555.8:c.857-21_857-20del	ENSP00000360610.4:n.857-21_857-20del
ENST00000371559.8:c.794-21_794-20del	ENSP00000360614.4:n.794-21_794-20del
ENST00000371560.4:c.857-21_857-20del	ENSP00000360615.3:n.857-21_857-20del
ENST00000371561.7:c.794-21_794-20del	ENSP00000360616.3:n.794-21_794-20del
ENST00000471122.5:n.871-21_871-20del
NM_000832.6:c.794-21_794-20del	NP_000823.4:n.794-21_794-20del
NM_001185090.1:c.857-21_857-20del	NP_001172019.1:n.857-21_857-20del
NM_001185091.1:c.857-21_857-20del	NP_001172020.1:n.857-21_857-20del
NM_007327.3:c.794-21_794-20del	NP_015566.1:n.794-21_794-20del
NM_021569.3:c.794-21_794-20del	NP_067544.1:n.794-21_794-20del
XM_005266071.2:c.794-21_794-20del	XP_005266128.1:n.794-21_794-20del
XM_005266072.2:c.857-21_857-20del	XP_005266129.1:n.857-21_857-20del
XM_005266073.3:c.857-21_857-20del	XP_005266130.1:n.857-21_857-20del
XM_011518583.1:c.857-21_857-20del	XP_011516885.1:n.857-21_857-20del
XM_005266071.3:c.794-21_794-20del	XP_005266128.1:n.794-21_794-20del
XM_005266072.3:c.857-21_857-20del	XP_005266129.1:n.857-21_857-20del
XM_005266073.4:c.857-21_857-20del	XP_005266130.1:n.857-21_857-20del
XM_011518583.2:c.857-21_857-20del	XP_011516885.1:n.857-21_857-20del
NM_007327.4:c.794-21_794-20del MANE Select	NP_015566.1:n.794-21_794-20del
NM_000832.7:c.794-21_794-20del	NP_000823.4:n.794-21_794-20del
NM_001185090.2:c.857-21_857-20del	NP_001172019.1:n.857-21_857-20del
NM_001185091.2:c.857-21_857-20del	NP_001172020.1:n.857-21_857-20del
NM_021569.4:c.794-21_794-20del	NP_067544.1:n.794-21_794-20del