Canonical Allele Identifier: CA2692783619

Gene: GRIN1

Linked Data

• gnomAD v4: 9-137163694-GGTGGGTTCTCC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137163700_137163710del , CM000671.2:g.137163700_137163710del	GRCh38
NC_000009.11:g.140058152_140058162del , CM000671.1:g.140058152_140058162del	GRCh37
NC_000009.10:g.139177973_139177983del	NCBI36
NG_011507.1:g.29544_29554del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371553.8:c.2506+32_2506+42del	ENSP00000360608.3:n.2506+32_2506+42del
ENST00000371560.5:c.2506+32_2506+42del	ENSP00000360615.3:n.2506+32_2506+42del
ENST00000371561.8:c.2443+32_2443+42del MANE Select	ENSP00000360616.3:n.2443+32_2443+42del
ENST00000675295.1:n.1873+32_1873+42del
ENST00000350902.9:c.*1418+32_*1418+42del	ENSP00000316915.9:n.*1418+32_*1418+42del
ENST00000371546.8:c.2506+32_2506+42del	ENSP00000360601.4:n.2506+32_2506+42del
ENST00000371550.8:c.2443+32_2443+42del	ENSP00000360605.4:n.2443+32_2443+42del
ENST00000371553.7:c.2506+32_2506+42del	ENSP00000360608.3:n.2506+32_2506+42del
ENST00000371555.8:c.2506+32_2506+42del	ENSP00000360610.4:n.2506+32_2506+42del
ENST00000371559.8:c.2443+32_2443+42del	ENSP00000360614.4:n.2443+32_2443+42del
ENST00000371560.4:c.2506+32_2506+42del	ENSP00000360615.3:n.2506+32_2506+42del
ENST00000371561.7:c.2443+32_2443+42del	ENSP00000360616.3:n.2443+32_2443+42del
ENST00000460273.1:n.464+32_464+42del
ENST00000471122.5:n.2520+32_2520+42del
NM_000832.6:c.2443+32_2443+42del	NP_000823.4:n.2443+32_2443+42del
NM_001185090.1:c.2506+32_2506+42del	NP_001172019.1:n.2506+32_2506+42del
NM_001185091.1:c.2506+32_2506+42del	NP_001172020.1:n.2506+32_2506+42del
NM_007327.3:c.2443+32_2443+42del	NP_015566.1:n.2443+32_2443+42del
NM_021569.3:c.2443+32_2443+42del	NP_067544.1:n.2443+32_2443+42del
XM_005266071.2:c.2443+32_2443+42del	XP_005266128.1:n.2443+32_2443+42del
XM_005266072.2:c.2506+32_2506+42del	XP_005266129.1:n.2506+32_2506+42del
XM_005266073.3:c.2506+32_2506+42del	XP_005266130.1:n.2506+32_2506+42del
XM_011518583.1:c.2506+32_2506+42del	XP_011516885.1:n.2506+32_2506+42del
XM_005266071.3:c.2443+32_2443+42del	XP_005266128.1:n.2443+32_2443+42del
XM_005266072.3:c.2506+32_2506+42del	XP_005266129.1:n.2506+32_2506+42del
XM_005266073.4:c.2506+32_2506+42del	XP_005266130.1:n.2506+32_2506+42del
XM_011518583.2:c.2506+32_2506+42del	XP_011516885.1:n.2506+32_2506+42del
NM_007327.4:c.2443+32_2443+42del MANE Select	NP_015566.1:n.2443+32_2443+42del
NM_000832.7:c.2443+32_2443+42del	NP_000823.4:n.2443+32_2443+42del
NM_001185090.2:c.2506+32_2506+42del	NP_001172019.1:n.2506+32_2506+42del
NM_001185091.2:c.2506+32_2506+42del	NP_001172020.1:n.2506+32_2506+42del
NM_021569.4:c.2443+32_2443+42del	NP_067544.1:n.2443+32_2443+42del