Canonical Allele Identifier: CA918579473

Gene: GRIN1

Linked Data

• dbSNP Id: rs1564365068

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137163545_137163546insGAA , CM000671.2:g.137163545_137163546insGAA	GRCh38
NC_000009.11:g.140057997_140057998insGAA , CM000671.1:g.140057997_140057998insGAA	GRCh37
NC_000009.10:g.139177818_139177819insGAA	NCBI36
NG_011507.1:g.29389_29390insGAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000371553.8:c.2397-14_2397-13insGAA	ENSP00000360608.3:n.2397-14_2397-13insGAA...
ENST00000371560.5:c.2397-14_2397-13insGAA	ENSP00000360615.3:n.2397-14_2397-13insGAA...
ENST00000371561.8:c.2334-14_2334-13insGAA MANE Select	ENSP00000360616.3:n.2334-14_2334-13insGAA...
ENST00000675295.1:n.1764-14_1764-13insGAA
ENST00000350902.9:c.*1309-14_*1309-13insGAA	ENSP00000316915.9:n.*1309-14_*1309-13insG...
ENST00000371546.8:c.2397-14_2397-13insGAA	ENSP00000360601.4:n.2397-14_2397-13insGAA...
ENST00000371550.8:c.2334-14_2334-13insGAA	ENSP00000360605.4:n.2334-14_2334-13insGAA...
ENST00000371553.7:c.2397-14_2397-13insGAA	ENSP00000360608.3:n.2397-14_2397-13insGAA...
ENST00000371555.8:c.2397-14_2397-13insGAA	ENSP00000360610.4:n.2397-14_2397-13insGAA...
ENST00000371559.8:c.2334-14_2334-13insGAA	ENSP00000360614.4:n.2334-14_2334-13insGAA...
ENST00000371560.4:c.2397-14_2397-13insGAA	ENSP00000360615.3:n.2397-14_2397-13insGAA...
ENST00000371561.7:c.2334-14_2334-13insGAA	ENSP00000360616.3:n.2334-14_2334-13insGAA...
ENST00000460273.1:n.355-14_355-13insGAA
ENST00000471122.5:n.2411-14_2411-13insGAA
NM_000832.6:c.2334-14_2334-13insGAA	NP_000823.4:n.2334-14_2334-13insGAA
NM_001185090.1:c.2397-14_2397-13insGAA	NP_001172019.1:n.2397-14_2397-13insGAA
NM_001185091.1:c.2397-14_2397-13insGAA	NP_001172020.1:n.2397-14_2397-13insGAA
NM_007327.3:c.2334-14_2334-13insGAA	NP_015566.1:n.2334-14_2334-13insGAA
NM_021569.3:c.2334-14_2334-13insGAA	NP_067544.1:n.2334-14_2334-13insGAA
XM_005266071.2:c.2334-14_2334-13insGAA	XP_005266128.1:n.2334-14_2334-13insGAA
XM_005266072.2:c.2397-14_2397-13insGAA	XP_005266129.1:n.2397-14_2397-13insGAA
XM_005266073.3:c.2397-14_2397-13insGAA	XP_005266130.1:n.2397-14_2397-13insGAA
XM_011518583.1:c.2397-14_2397-13insGAA	XP_011516885.1:n.2397-14_2397-13insGAA
XM_005266071.3:c.2334-14_2334-13insGAA	XP_005266128.1:n.2334-14_2334-13insGAA
XM_005266072.3:c.2397-14_2397-13insGAA	XP_005266129.1:n.2397-14_2397-13insGAA
XM_005266073.4:c.2397-14_2397-13insGAA	XP_005266130.1:n.2397-14_2397-13insGAA
XM_011518583.2:c.2397-14_2397-13insGAA	XP_011516885.1:n.2397-14_2397-13insGAA
NM_007327.4:c.2334-14_2334-13insGAA MANE Select	NP_015566.1:n.2334-14_2334-13insGAA
NM_000832.7:c.2334-14_2334-13insGAA	NP_000823.4:n.2334-14_2334-13insGAA
NM_001185090.2:c.2397-14_2397-13insGAA	NP_001172019.1:n.2397-14_2397-13insGAA
NM_001185091.2:c.2397-14_2397-13insGAA	NP_001172020.1:n.2397-14_2397-13insGAA
NM_021569.4:c.2334-14_2334-13insGAA	NP_067544.1:n.2334-14_2334-13insGAA