Canonical Allele Identifier: CA2663623800

Gene: CHRNG

Linked Data

• gnomAD v4: 2-232541659-T-TGTGCCCCATGTGGATAG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232541660_232541661insTGCCCCATGTGGATAGG , CM000664.2:g.232541660_232541661insTGCCCCATGTGGATAGG	GRCh38
NC_000002.11:g.233406370_233406371insTGCCCCATGTGGATAGG , CM000664.1:g.233406370_233406371insTGCCCCATGTGGATAGG	GRCh37
NC_000002.10:g.233114614_233114615insTGCCCCATGTGGATAGG	NCBI36
NG_012954.1:g.6934_6935insTGCCCCATGTGGATAGG
NG_012954.2:g.6969_6970insTGCCCCATGTGGATAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651502.1:c.506+131_506+132insTGCCCCATGTGGATAGG MANE Select	ENSP00000498757.1:n.506+131_506+132insTGCCCCATGTGGATAGG
ENST00000389492.3:c.351-763_351-762insTGCCCCATGTGGATAGG	ENSP00000374143.3:n.351-763_351-762insTGCCCCATGTGGATAGG
ENST00000389494.7:c.506+131_506+132insTGCCCCATGTGGATAGG	ENSP00000374145.3:n.506+131_506+132insTGCCCCATGTGGATAGG
ENST00000485094.1:n.658_659insTGCCCCATGTGGATAGG
NM_005199.4:c.506+131_506+132insTGCCCCATGTGGATAGG	NP_005190.4:n.506+131_506+132insTGCCCCATGTGGATAGG
NM_005199.5:c.506+131_506+132insTGCCCCATGTGGATAGG MANE Select	NP_005190.4:n.506+131_506+132insTGCCCCATGTGGATAGG