Canonical Allele Identifier: CA1884331030

Gene: GRIN1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137162757_137162758delinsTG , CM000671.2:g.137162757_137162758delinsTG	GRCh38
NC_000009.11:g.140057209_140057210delinsTG , CM000671.1:g.140057209_140057210delinsTG	GRCh37
NC_000009.10:g.139177030_139177031delinsTG	NCBI36
NG_011507.1:g.28601_28602delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371553.8:c.2076+18_2076+19delinsTG	ENSP00000360608.3:n.2076+18_2076+19delinsTG
ENST00000371560.5:c.2076+18_2076+19delinsTG	ENSP00000360615.3:n.2076+18_2076+19delinsTG
ENST00000371561.8:c.2013+18_2013+19delinsTG MANE Select	ENSP00000360616.3:n.2013+18_2013+19delinsTG
ENST00000675295.1:n.1443+18_1443+19delinsTG
ENST00000350902.9:c.*988+18_*988+19delinsTG	ENSP00000316915.9:n.*988+18_*988+19delinsTG
ENST00000371546.8:c.2076+18_2076+19delinsTG	ENSP00000360601.4:n.2076+18_2076+19delinsTG
ENST00000371550.8:c.2013+18_2013+19delinsTG	ENSP00000360605.4:n.2013+18_2013+19delinsTG
ENST00000371553.7:c.2076+18_2076+19delinsTG	ENSP00000360608.3:n.2076+18_2076+19delinsTG
ENST00000371555.8:c.2076+18_2076+19delinsTG	ENSP00000360610.4:n.2076+18_2076+19delinsTG
ENST00000371559.8:c.2013+18_2013+19delinsTG	ENSP00000360614.4:n.2013+18_2013+19delinsTG
ENST00000371560.4:c.2076+18_2076+19delinsTG	ENSP00000360615.3:n.2076+18_2076+19delinsTG
ENST00000371561.7:c.2013+18_2013+19delinsTG	ENSP00000360616.3:n.2013+18_2013+19delinsTG
ENST00000460273.1:n.34+18_34+19delinsTG
ENST00000471122.5:n.2090+18_2090+19delinsTG
NM_000832.6:c.2013+18_2013+19delinsTG	NP_000823.4:n.2013+18_2013+19delinsTG
NM_001185090.1:c.2076+18_2076+19delinsTG	NP_001172019.1:n.2076+18_2076+19delinsTG
NM_001185091.1:c.2076+18_2076+19delinsTG	NP_001172020.1:n.2076+18_2076+19delinsTG
NM_007327.3:c.2013+18_2013+19delinsTG	NP_015566.1:n.2013+18_2013+19delinsTG
NM_021569.3:c.2013+18_2013+19delinsTG	NP_067544.1:n.2013+18_2013+19delinsTG
XM_005266071.2:c.2013+18_2013+19delinsTG	XP_005266128.1:n.2013+18_2013+19delinsTG
XM_005266072.2:c.2076+18_2076+19delinsTG	XP_005266129.1:n.2076+18_2076+19delinsTG
XM_005266073.3:c.2076+18_2076+19delinsTG	XP_005266130.1:n.2076+18_2076+19delinsTG
XM_011518583.1:c.2076+18_2076+19delinsTG	XP_011516885.1:n.2076+18_2076+19delinsTG
XM_005266071.3:c.2013+18_2013+19delinsTG	XP_005266128.1:n.2013+18_2013+19delinsTG
XM_005266072.3:c.2076+18_2076+19delinsTG	XP_005266129.1:n.2076+18_2076+19delinsTG
XM_005266073.4:c.2076+18_2076+19delinsTG	XP_005266130.1:n.2076+18_2076+19delinsTG
XM_011518583.2:c.2076+18_2076+19delinsTG	XP_011516885.1:n.2076+18_2076+19delinsTG
NM_007327.4:c.2013+18_2013+19delinsTG MANE Select	NP_015566.1:n.2013+18_2013+19delinsTG
NM_000832.7:c.2013+18_2013+19delinsTG	NP_000823.4:n.2013+18_2013+19delinsTG
NM_001185090.2:c.2076+18_2076+19delinsTG	NP_001172019.1:n.2076+18_2076+19delinsTG
NM_001185091.2:c.2076+18_2076+19delinsTG	NP_001172020.1:n.2076+18_2076+19delinsTG
NM_021569.4:c.2013+18_2013+19delinsTG	NP_067544.1:n.2013+18_2013+19delinsTG