Canonical Allele Identifier: CA2663621459

Gene: CHRNG

Linked Data

• gnomAD v4: 2-232539872-T-TCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232539873_232539874insCCC , CM000664.2:g.232539873_232539874insCCC	GRCh38
NC_000002.11:g.233404583_233404584insCCC , CM000664.1:g.233404583_233404584insCCC	GRCh37
NC_000002.10:g.233112827_233112828insCCC	NCBI36
NG_012954.1:g.5147_5148insCCC
NG_012954.2:g.5182_5183insCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651502.1:c.55+71_55+72insCCC MANE Select	ENSP00000498757.1:n.55+71_55+72insCCC
ENST00000389492.3:c.55+71_55+72insCCC	ENSP00000374143.3:n.55+71_55+72insCCC
ENST00000389494.7:c.55+71_55+72insCCC	ENSP00000374145.3:n.55+71_55+72insCCC
ENST00000485094.1:n.76+71_76+72insCCC
NM_005199.4:c.55+71_55+72insCCC	NP_005190.4:n.55+71_55+72insCCC
NM_005199.5:c.55+71_55+72insCCC MANE Select	NP_005190.4:n.55+71_55+72insCCC