Canonical Allele Identifier: CA2739265230

Gene: GRIN1

Linked Data

• ClinVar Variation Id: 2835750
• ClinVar RCV Id: RCV003644028

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137163757_137163763del , CM000671.2:g.137163757_137163763del	GRCh38
NC_000009.11:g.140058209_140058215del , CM000671.1:g.140058209_140058215del	GRCh37
NC_000009.10:g.139178030_139178036del	NCBI36
NG_011507.1:g.29601_29607del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371553.8:c.2507-2_2511del
ENST00000371560.5:c.2507-2_2511del
ENST00000371561.8:c.2444-2_2448del
ENST00000675295.1:n.1874-2_1878del
ENST00000350902.9:c.*1419-2_*1423del
ENST00000371546.8:c.2507-2_2511del
ENST00000371550.8:c.2444-2_2448del
ENST00000371553.7:c.2507-2_2511del
ENST00000371555.8:c.2507-2_2511del
ENST00000371559.8:c.2444-2_2448del
ENST00000371560.4:c.2507-2_2511del
ENST00000371561.7:c.2444-2_2448del
ENST00000460273.1:n.465-2_469del
ENST00000471122.5:n.2521-2_2525del
NM_000832.6:c.2444-2_2448del
NM_001185090.1:c.2507-2_2511del
NM_001185091.1:c.2507-2_2511del
NM_007327.3:c.2444-2_2448del
NM_021569.3:c.2444-2_2448del
XM_005266071.2:c.2444-2_2448del
XM_005266072.2:c.2507-2_2511del
XM_005266073.3:c.2507-2_2511del
XM_011518583.1:c.2507-2_2511del
XM_005266071.3:c.2444-2_2448del
XM_005266072.3:c.2507-2_2511del
XM_005266073.4:c.2507-2_2511del
XM_011518583.2:c.2507-2_2511del
NM_007327.4:c.2444-2_2448del
NM_000832.7:c.2444-2_2448del
NM_001185090.2:c.2507-2_2511del
NM_001185091.2:c.2507-2_2511del
NM_021569.4:c.2444-2_2448del