Canonical Allele Identifier: CA2692782416

Gene: GRIN1

Linked Data

• gnomAD v4: 9-137162304-GGGGCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137162305_137162309del , CM000671.2:g.137162305_137162309del	GRCh38
NC_000009.11:g.140056757_140056761del , CM000671.1:g.140056757_140056761del	GRCh37
NC_000009.10:g.139176578_139176582del	NCBI36
NG_011507.1:g.28149_28153del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371553.8:c.1814+15_1814+19del	ENSP00000360608.3:n.1814+15_1814+19del
ENST00000371560.5:c.1814+15_1814+19del	ENSP00000360615.3:n.1814+15_1814+19del
ENST00000371561.8:c.1751+15_1751+19del MANE Select	ENSP00000360616.3:n.1751+15_1751+19del
ENST00000675295.1:n.1181+15_1181+19del
ENST00000350902.9:c.*726+15_*726+19del	ENSP00000316915.9:n.*726+15_*726+19del
ENST00000371546.8:c.1814+15_1814+19del	ENSP00000360601.4:n.1814+15_1814+19del
ENST00000371550.8:c.1751+15_1751+19del	ENSP00000360605.4:n.1751+15_1751+19del
ENST00000371553.7:c.1814+15_1814+19del	ENSP00000360608.3:n.1814+15_1814+19del
ENST00000371555.8:c.1814+15_1814+19del	ENSP00000360610.4:n.1814+15_1814+19del
ENST00000371559.8:c.1751+15_1751+19del	ENSP00000360614.4:n.1751+15_1751+19del
ENST00000371560.4:c.1814+15_1814+19del	ENSP00000360615.3:n.1814+15_1814+19del
ENST00000371561.7:c.1751+15_1751+19del	ENSP00000360616.3:n.1751+15_1751+19del
ENST00000471122.5:n.1828+15_1828+19del
NM_000832.6:c.1751+15_1751+19del	NP_000823.4:n.1751+15_1751+19del
NM_001185090.1:c.1814+15_1814+19del	NP_001172019.1:n.1814+15_1814+19del
NM_001185091.1:c.1814+15_1814+19del	NP_001172020.1:n.1814+15_1814+19del
NM_007327.3:c.1751+15_1751+19del	NP_015566.1:n.1751+15_1751+19del
NM_021569.3:c.1751+15_1751+19del	NP_067544.1:n.1751+15_1751+19del
XM_005266071.2:c.1751+15_1751+19del	XP_005266128.1:n.1751+15_1751+19del
XM_005266072.2:c.1814+15_1814+19del	XP_005266129.1:n.1814+15_1814+19del
XM_005266073.3:c.1814+15_1814+19del	XP_005266130.1:n.1814+15_1814+19del
XM_011518583.1:c.1814+15_1814+19del	XP_011516885.1:n.1814+15_1814+19del
XM_005266071.3:c.1751+15_1751+19del	XP_005266128.1:n.1751+15_1751+19del
XM_005266072.3:c.1814+15_1814+19del	XP_005266129.1:n.1814+15_1814+19del
XM_005266073.4:c.1814+15_1814+19del	XP_005266130.1:n.1814+15_1814+19del
XM_011518583.2:c.1814+15_1814+19del	XP_011516885.1:n.1814+15_1814+19del
NM_007327.4:c.1751+15_1751+19del MANE Select	NP_015566.1:n.1751+15_1751+19del
NM_000832.7:c.1751+15_1751+19del	NP_000823.4:n.1751+15_1751+19del
NM_001185090.2:c.1814+15_1814+19del	NP_001172019.1:n.1814+15_1814+19del
NM_001185091.2:c.1814+15_1814+19del	NP_001172020.1:n.1814+15_1814+19del
NM_021569.4:c.1751+15_1751+19del	NP_067544.1:n.1751+15_1751+19del