Canonical Allele Identifier: CA2692782468

Gene: GRIN1

Linked Data

• gnomAD v4: 9-137162325-G-GAGCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137162325_137162326insAGCCC , CM000671.2:g.137162325_137162326insAGCCC	GRCh38
NC_000009.11:g.140056777_140056778insAGCCC , CM000671.1:g.140056777_140056778insAGCCC	GRCh37
NC_000009.10:g.139176598_139176599insAGCCC	NCBI36
NG_011507.1:g.28169_28170insAGCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371553.8:c.1814+35_1814+36insAGCCC	ENSP00000360608.3:n.1814+35_1814+36insAGCCC
ENST00000371560.5:c.1814+35_1814+36insAGCCC	ENSP00000360615.3:n.1814+35_1814+36insAGCCC
ENST00000371561.8:c.1751+35_1751+36insAGCCC MANE Select	ENSP00000360616.3:n.1751+35_1751+36insAGCCC
ENST00000675295.1:n.1181+35_1181+36insAGCCC
ENST00000350902.9:c.*726+35_*726+36insAGCCC	ENSP00000316915.9:n.*726+35_*726+36insAGCCC
ENST00000371546.8:c.1814+35_1814+36insAGCCC	ENSP00000360601.4:n.1814+35_1814+36insAGCCC
ENST00000371550.8:c.1751+35_1751+36insAGCCC	ENSP00000360605.4:n.1751+35_1751+36insAGCCC
ENST00000371553.7:c.1814+35_1814+36insAGCCC	ENSP00000360608.3:n.1814+35_1814+36insAGCCC
ENST00000371555.8:c.1814+35_1814+36insAGCCC	ENSP00000360610.4:n.1814+35_1814+36insAGCCC
ENST00000371559.8:c.1751+35_1751+36insAGCCC	ENSP00000360614.4:n.1751+35_1751+36insAGCCC
ENST00000371560.4:c.1814+35_1814+36insAGCCC	ENSP00000360615.3:n.1814+35_1814+36insAGCCC
ENST00000371561.7:c.1751+35_1751+36insAGCCC	ENSP00000360616.3:n.1751+35_1751+36insAGCCC
ENST00000471122.5:n.1828+35_1828+36insAGCCC
NM_000832.6:c.1751+35_1751+36insAGCCC	NP_000823.4:n.1751+35_1751+36insAGCCC
NM_001185090.1:c.1814+35_1814+36insAGCCC	NP_001172019.1:n.1814+35_1814+36insAGCCC
NM_001185091.1:c.1814+35_1814+36insAGCCC	NP_001172020.1:n.1814+35_1814+36insAGCCC
NM_007327.3:c.1751+35_1751+36insAGCCC	NP_015566.1:n.1751+35_1751+36insAGCCC
NM_021569.3:c.1751+35_1751+36insAGCCC	NP_067544.1:n.1751+35_1751+36insAGCCC
XM_005266071.2:c.1751+35_1751+36insAGCCC	XP_005266128.1:n.1751+35_1751+36insAGCCC
XM_005266072.2:c.1814+35_1814+36insAGCCC	XP_005266129.1:n.1814+35_1814+36insAGCCC
XM_005266073.3:c.1814+35_1814+36insAGCCC	XP_005266130.1:n.1814+35_1814+36insAGCCC
XM_011518583.1:c.1814+35_1814+36insAGCCC	XP_011516885.1:n.1814+35_1814+36insAGCCC
XM_005266071.3:c.1751+35_1751+36insAGCCC	XP_005266128.1:n.1751+35_1751+36insAGCCC
XM_005266072.3:c.1814+35_1814+36insAGCCC	XP_005266129.1:n.1814+35_1814+36insAGCCC
XM_005266073.4:c.1814+35_1814+36insAGCCC	XP_005266130.1:n.1814+35_1814+36insAGCCC
XM_011518583.2:c.1814+35_1814+36insAGCCC	XP_011516885.1:n.1814+35_1814+36insAGCCC
NM_007327.4:c.1751+35_1751+36insAGCCC MANE Select	NP_015566.1:n.1751+35_1751+36insAGCCC
NM_000832.7:c.1751+35_1751+36insAGCCC	NP_000823.4:n.1751+35_1751+36insAGCCC
NM_001185090.2:c.1814+35_1814+36insAGCCC	NP_001172019.1:n.1814+35_1814+36insAGCCC
NM_001185091.2:c.1814+35_1814+36insAGCCC	NP_001172020.1:n.1814+35_1814+36insAGCCC
NM_021569.4:c.1751+35_1751+36insAGCCC	NP_067544.1:n.1751+35_1751+36insAGCCC