Canonical Allele Identifier: CA1884330819

Gene: GRIN1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137162365_137162366delinsCT , CM000671.2:g.137162365_137162366delinsCT	GRCh38
NC_000009.11:g.140056817_140056818delinsCT , CM000671.1:g.140056817_140056818delinsCT	GRCh37
NC_000009.10:g.139176638_139176639delinsCT	NCBI36
NG_011507.1:g.28209_28210delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371553.8:c.1815-39_1815-38delinsCT	ENSP00000360608.3:n.1815-39_1815-38delinsCT
ENST00000371560.5:c.1815-39_1815-38delinsCT	ENSP00000360615.3:n.1815-39_1815-38delinsCT
ENST00000371561.8:c.1752-39_1752-38delinsCT MANE Select	ENSP00000360616.3:n.1752-39_1752-38delinsCT
ENST00000675295.1:n.1182-39_1182-38delinsCT
ENST00000350902.9:c.*727-39_*727-38delinsCT	ENSP00000316915.9:n.*727-39_*727-38delinsCT
ENST00000371546.8:c.1815-39_1815-38delinsCT	ENSP00000360601.4:n.1815-39_1815-38delinsCT
ENST00000371550.8:c.1752-39_1752-38delinsCT	ENSP00000360605.4:n.1752-39_1752-38delinsCT
ENST00000371553.7:c.1815-39_1815-38delinsCT	ENSP00000360608.3:n.1815-39_1815-38delinsCT
ENST00000371555.8:c.1815-39_1815-38delinsCT	ENSP00000360610.4:n.1815-39_1815-38delinsCT
ENST00000371559.8:c.1752-39_1752-38delinsCT	ENSP00000360614.4:n.1752-39_1752-38delinsCT
ENST00000371560.4:c.1815-39_1815-38delinsCT	ENSP00000360615.3:n.1815-39_1815-38delinsCT
ENST00000371561.7:c.1752-39_1752-38delinsCT	ENSP00000360616.3:n.1752-39_1752-38delinsCT
ENST00000471122.5:n.1829-39_1829-38delinsCT
NM_000832.6:c.1752-39_1752-38delinsCT	NP_000823.4:n.1752-39_1752-38delinsCT
NM_001185090.1:c.1815-39_1815-38delinsCT	NP_001172019.1:n.1815-39_1815-38delinsCT
NM_001185091.1:c.1815-39_1815-38delinsCT	NP_001172020.1:n.1815-39_1815-38delinsCT
NM_007327.3:c.1752-39_1752-38delinsCT	NP_015566.1:n.1752-39_1752-38delinsCT
NM_021569.3:c.1752-39_1752-38delinsCT	NP_067544.1:n.1752-39_1752-38delinsCT
XM_005266071.2:c.1752-39_1752-38delinsCT	XP_005266128.1:n.1752-39_1752-38delinsCT
XM_005266072.2:c.1815-39_1815-38delinsCT	XP_005266129.1:n.1815-39_1815-38delinsCT
XM_005266073.3:c.1815-39_1815-38delinsCT	XP_005266130.1:n.1815-39_1815-38delinsCT
XM_011518583.1:c.1815-39_1815-38delinsCT	XP_011516885.1:n.1815-39_1815-38delinsCT
XM_005266071.3:c.1752-39_1752-38delinsCT	XP_005266128.1:n.1752-39_1752-38delinsCT
XM_005266072.3:c.1815-39_1815-38delinsCT	XP_005266129.1:n.1815-39_1815-38delinsCT
XM_005266073.4:c.1815-39_1815-38delinsCT	XP_005266130.1:n.1815-39_1815-38delinsCT
XM_011518583.2:c.1815-39_1815-38delinsCT	XP_011516885.1:n.1815-39_1815-38delinsCT
NM_007327.4:c.1752-39_1752-38delinsCT MANE Select	NP_015566.1:n.1752-39_1752-38delinsCT
NM_000832.7:c.1752-39_1752-38delinsCT	NP_000823.4:n.1752-39_1752-38delinsCT
NM_001185090.2:c.1815-39_1815-38delinsCT	NP_001172019.1:n.1815-39_1815-38delinsCT
NM_001185091.2:c.1815-39_1815-38delinsCT	NP_001172020.1:n.1815-39_1815-38delinsCT
NM_021569.4:c.1752-39_1752-38delinsCT	NP_067544.1:n.1752-39_1752-38delinsCT