Canonical Allele Identifier: CA2663623809

Gene: CHRNG

Linked Data

• gnomAD v4: 2-232541664-C-CTGGGGACACCAG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232541665_232541666insGGGGACACCAGT , CM000664.2:g.232541665_232541666insGGGGACACCAGT	GRCh38
NC_000002.11:g.233406375_233406376insGGGGACACCAGT , CM000664.1:g.233406375_233406376insGGGGACACCAGT	GRCh37
NC_000002.10:g.233114619_233114620insGGGGACACCAGT	NCBI36
NG_012954.1:g.6939_6940insGGGGACACCAGT
NG_012954.2:g.6974_6975insGGGGACACCAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651502.1:c.506+136_506+137insGGGGACACCAGT MANE Select	ENSP00000498757.1:n.506+136_506+137insGGGGACACCAGT
ENST00000389492.3:c.351-758_351-757insGGGGACACCAGT	ENSP00000374143.3:n.351-758_351-757insGGGGACACCAGT
ENST00000389494.7:c.506+136_506+137insGGGGACACCAGT	ENSP00000374145.3:n.506+136_506+137insGGGGACACCAGT
ENST00000485094.1:n.663_664insGGGGACACCAGT
NM_005199.4:c.506+136_506+137insGGGGACACCAGT	NP_005190.4:n.506+136_506+137insGGGGACACCAGT
NM_005199.5:c.506+136_506+137insGGGGACACCAGT MANE Select	NP_005190.4:n.506+136_506+137insGGGGACACCAGT