Canonical Allele Identifier: CA2663621513

Gene: CHRNG

Linked Data

• gnomAD v4: 2-232539905-T-TGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232539905_232539906insGGG , CM000664.2:g.232539905_232539906insGGG	GRCh38
NC_000002.11:g.233404615_233404616insGGG , CM000664.1:g.233404615_233404616insGGG	GRCh37
NC_000002.10:g.233112859_233112860insGGG	NCBI36
NG_012954.1:g.5179_5180insGGG
NG_012954.2:g.5214_5215insGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651502.1:c.56-87_56-86insGGG MANE Select	ENSP00000498757.1:n.56-87_56-86insGGG
ENST00000389492.3:c.56-87_56-86insGGG	ENSP00000374143.3:n.56-87_56-86insGGG
ENST00000389494.7:c.56-87_56-86insGGG	ENSP00000374145.3:n.56-87_56-86insGGG
ENST00000485094.1:n.77-87_77-86insGGG
NM_005199.4:c.56-87_56-86insGGG	NP_005190.4:n.56-87_56-86insGGG
NM_005199.5:c.56-87_56-86insGGG MANE Select	NP_005190.4:n.56-87_56-86insGGG