Canonical Allele Identifier: CA1884330535

Gene: GRIN1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137161694_137161701delinsGAGTGGGC , CM000671.2:g.137161694_137161701delinsGAGTGGGC	GRCh38
NC_000009.11:g.140056146_140056153delinsGAGTGGGC , CM000671.1:g.140056146_140056153delinsGAGTGGGC	GRCh37
NC_000009.10:g.139175967_139175974delinsGAGTGGGC	NCBI36
NG_011507.1:g.27538_27545delinsGAGTGGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371553.8:c.1531-230_1531-223delinsGAGTGGGC	ENSP00000360608.3:n.1531-230_1531-223delinsGAGTGGGC
ENST00000371560.5:c.1531-230_1531-223delinsGAGTGGGC	ENSP00000360615.3:n.1531-230_1531-223delinsGAGTGGGC
ENST00000371561.8:c.1468-230_1468-223delinsGAGTGGGC MANE Select	ENSP00000360616.3:n.1468-230_1468-223delinsGAGTGGGC
ENST00000675295.1:n.898-230_898-223delinsGAGTGGGC
ENST00000350902.9:c.*443-230_*443-223delinsGAGTGGGC	ENSP00000316915.9:n.*443-230_*443-223delinsGAGTGGGC
ENST00000371546.8:c.1531-230_1531-223delinsGAGTGGGC	ENSP00000360601.4:n.1531-230_1531-223delinsGAGTGGGC
ENST00000371550.8:c.1468-230_1468-223delinsGAGTGGGC	ENSP00000360605.4:n.1468-230_1468-223delinsGAGTGGGC
ENST00000371553.7:c.1531-230_1531-223delinsGAGTGGGC	ENSP00000360608.3:n.1531-230_1531-223delinsGAGTGGGC
ENST00000371555.8:c.1531-230_1531-223delinsGAGTGGGC	ENSP00000360610.4:n.1531-230_1531-223delinsGAGTGGGC
ENST00000371559.8:c.1468-230_1468-223delinsGAGTGGGC	ENSP00000360614.4:n.1468-230_1468-223delinsGAGTGGGC
ENST00000371560.4:c.1531-230_1531-223delinsGAGTGGGC	ENSP00000360615.3:n.1531-230_1531-223delinsGAGTGGGC
ENST00000371561.7:c.1468-230_1468-223delinsGAGTGGGC	ENSP00000360616.3:n.1468-230_1468-223delinsGAGTGGGC
ENST00000471122.5:n.1545-230_1545-223delinsGAGTGGGC
NM_000832.6:c.1468-230_1468-223delinsGAGTGGGC	NP_000823.4:n.1468-230_1468-223delinsGAGTGGGC
NM_001185090.1:c.1531-230_1531-223delinsGAGTGGGC	NP_001172019.1:n.1531-230_1531-223delinsGAGTGGGC
NM_001185091.1:c.1531-230_1531-223delinsGAGTGGGC	NP_001172020.1:n.1531-230_1531-223delinsGAGTGGGC
NM_007327.3:c.1468-230_1468-223delinsGAGTGGGC	NP_015566.1:n.1468-230_1468-223delinsGAGTGGGC
NM_021569.3:c.1468-230_1468-223delinsGAGTGGGC	NP_067544.1:n.1468-230_1468-223delinsGAGTGGGC
XM_005266071.2:c.1468-230_1468-223delinsGAGTGGGC	XP_005266128.1:n.1468-230_1468-223delinsGAGTGGGC
XM_005266072.2:c.1531-230_1531-223delinsGAGTGGGC	XP_005266129.1:n.1531-230_1531-223delinsGAGTGGGC
XM_005266073.3:c.1531-230_1531-223delinsGAGTGGGC	XP_005266130.1:n.1531-230_1531-223delinsGAGTGGGC
XM_011518583.1:c.1531-230_1531-223delinsGAGTGGGC	XP_011516885.1:n.1531-230_1531-223delinsGAGTGGGC
XM_005266071.3:c.1468-230_1468-223delinsGAGTGGGC	XP_005266128.1:n.1468-230_1468-223delinsGAGTGGGC
XM_005266072.3:c.1531-230_1531-223delinsGAGTGGGC	XP_005266129.1:n.1531-230_1531-223delinsGAGTGGGC
XM_005266073.4:c.1531-230_1531-223delinsGAGTGGGC	XP_005266130.1:n.1531-230_1531-223delinsGAGTGGGC
XM_011518583.2:c.1531-230_1531-223delinsGAGTGGGC	XP_011516885.1:n.1531-230_1531-223delinsGAGTGGGC
NM_007327.4:c.1468-230_1468-223delinsGAGTGGGC MANE Select	NP_015566.1:n.1468-230_1468-223delinsGAGTGGGC
NM_000832.7:c.1468-230_1468-223delinsGAGTGGGC	NP_000823.4:n.1468-230_1468-223delinsGAGTGGGC
NM_001185090.2:c.1531-230_1531-223delinsGAGTGGGC	NP_001172019.1:n.1531-230_1531-223delinsGAGTGGGC
NM_001185091.2:c.1531-230_1531-223delinsGAGTGGGC	NP_001172020.1:n.1531-230_1531-223delinsGAGTGGGC
NM_021569.4:c.1468-230_1468-223delinsGAGTGGGC	NP_067544.1:n.1468-230_1468-223delinsGAGTGGGC