Canonical Allele Identifier: CA2663623784

Gene: CHRNG

Linked Data

• gnomAD v4: 2-232541654-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232541658del , CM000664.2:g.232541658del	GRCh38
NC_000002.11:g.233406368del , CM000664.1:g.233406368del	GRCh37
NC_000002.10:g.233114612del	NCBI36
NG_012954.1:g.6932del
NG_012954.2:g.6967del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651502.1:c.506+129del MANE Select	ENSP00000498757.1:n.506+129del
ENST00000389492.3:c.351-765del	ENSP00000374143.3:n.351-765del
ENST00000389494.7:c.506+129del	ENSP00000374145.3:n.506+129del
ENST00000485094.1:n.656del
NM_005199.4:c.506+129del	NP_005190.4:n.506+129del
NM_005199.5:c.506+129del MANE Select	NP_005190.4:n.506+129del