Canonical Allele Identifier: CA2663621511

Gene: CHRNG

Linked Data

• gnomAD v4: 2-232539904-G-GGGAAC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232539904_232539905insGGAAC , CM000664.2:g.232539904_232539905insGGAAC	GRCh38
NC_000002.11:g.233404614_233404615insGGAAC , CM000664.1:g.233404614_233404615insGGAAC	GRCh37
NC_000002.10:g.233112858_233112859insGGAAC	NCBI36
NG_012954.1:g.5178_5179insGGAAC
NG_012954.2:g.5213_5214insGGAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651502.1:c.56-88_56-87insGGAAC MANE Select	ENSP00000498757.1:n.56-88_56-87insGGAAC
ENST00000389492.3:c.56-88_56-87insGGAAC	ENSP00000374143.3:n.56-88_56-87insGGAAC
ENST00000389494.7:c.56-88_56-87insGGAAC	ENSP00000374145.3:n.56-88_56-87insGGAAC
ENST00000485094.1:n.77-88_77-87insGGAAC
NM_005199.4:c.56-88_56-87insGGAAC	NP_005190.4:n.56-88_56-87insGGAAC
NM_005199.5:c.56-88_56-87insGGAAC MANE Select	NP_005190.4:n.56-88_56-87insGGAAC