Canonical Allele Identifier: CA2720957349

Gene: GRIN1

Linked Data

• dbSNP Id: rs2131302425

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137163542_137163543del , CM000671.2:g.137163542_137163543del	GRCh38
NC_000009.11:g.140057994_140057995del , CM000671.1:g.140057994_140057995del	GRCh37
NC_000009.10:g.139177815_139177816del	NCBI36
NG_011507.1:g.29386_29387del

Transcript Alleles

HGVS	Amino-acid change
ENST00000371553.8:c.2397-17_2397-16del	ENSP00000360608.3:n.2397-17_2397-16del
ENST00000371560.5:c.2397-17_2397-16del	ENSP00000360615.3:n.2397-17_2397-16del
ENST00000371561.8:c.2334-17_2334-16del MANE Select	ENSP00000360616.3:n.2334-17_2334-16del
ENST00000675295.1:n.1764-17_1764-16del
ENST00000350902.9:c.*1309-17_*1309-16del	ENSP00000316915.9:n.*1309-17_*1309-16del
ENST00000371546.8:c.2397-17_2397-16del	ENSP00000360601.4:n.2397-17_2397-16del
ENST00000371550.8:c.2334-17_2334-16del	ENSP00000360605.4:n.2334-17_2334-16del
ENST00000371553.7:c.2397-17_2397-16del	ENSP00000360608.3:n.2397-17_2397-16del
ENST00000371555.8:c.2397-17_2397-16del	ENSP00000360610.4:n.2397-17_2397-16del
ENST00000371559.8:c.2334-17_2334-16del	ENSP00000360614.4:n.2334-17_2334-16del
ENST00000371560.4:c.2397-17_2397-16del	ENSP00000360615.3:n.2397-17_2397-16del
ENST00000371561.7:c.2334-17_2334-16del	ENSP00000360616.3:n.2334-17_2334-16del
ENST00000460273.1:n.355-17_355-16del
ENST00000471122.5:n.2411-17_2411-16del
NM_000832.6:c.2334-17_2334-16del	NP_000823.4:n.2334-17_2334-16del
NM_001185090.1:c.2397-17_2397-16del	NP_001172019.1:n.2397-17_2397-16del
NM_001185091.1:c.2397-17_2397-16del	NP_001172020.1:n.2397-17_2397-16del
NM_007327.3:c.2334-17_2334-16del	NP_015566.1:n.2334-17_2334-16del
NM_021569.3:c.2334-17_2334-16del	NP_067544.1:n.2334-17_2334-16del
XM_005266071.2:c.2334-17_2334-16del	XP_005266128.1:n.2334-17_2334-16del
XM_005266072.2:c.2397-17_2397-16del	XP_005266129.1:n.2397-17_2397-16del
XM_005266073.3:c.2397-17_2397-16del	XP_005266130.1:n.2397-17_2397-16del
XM_011518583.1:c.2397-17_2397-16del	XP_011516885.1:n.2397-17_2397-16del
XM_005266071.3:c.2334-17_2334-16del	XP_005266128.1:n.2334-17_2334-16del
XM_005266072.3:c.2397-17_2397-16del	XP_005266129.1:n.2397-17_2397-16del
XM_005266073.4:c.2397-17_2397-16del	XP_005266130.1:n.2397-17_2397-16del
XM_011518583.2:c.2397-17_2397-16del	XP_011516885.1:n.2397-17_2397-16del
NM_007327.4:c.2334-17_2334-16del MANE Select	NP_015566.1:n.2334-17_2334-16del
NM_000832.7:c.2334-17_2334-16del	NP_000823.4:n.2334-17_2334-16del
NM_001185090.2:c.2397-17_2397-16del	NP_001172019.1:n.2397-17_2397-16del
NM_001185091.2:c.2397-17_2397-16del	NP_001172020.1:n.2397-17_2397-16del
NM_021569.4:c.2334-17_2334-16del	NP_067544.1:n.2334-17_2334-16del