Canonical Allele Identifier: CA2663621443

Gene: CHRNG

Linked Data

• gnomAD v4: 2-232539860-G-GACCCTCCATCCCCTGAGGCTGT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232539860_232539861insACCCTCCATCCCCTGAGGCTGT , CM000664.2:g.232539860_232539861insACCCTCCATCCCCTGAGGCTGT	GRCh38
NC_000002.11:g.233404570_233404571insACCCTCCATCCCCTGAGGCTGT , CM000664.1:g.233404570_233404571insACCCTCCATCCCCTGAGGCTGT	GRCh37
NC_000002.10:g.233112814_233112815insACCCTCCATCCCCTGAGGCTGT	NCBI36
NG_012954.1:g.5134_5135insACCCTCCATCCCCTGAGGCTGT
NG_012954.2:g.5169_5170insACCCTCCATCCCCTGAGGCTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651502.1:c.55+58_55+59insACCCTCCATCCCCTGAGGCTGT MANE Select	ENSP00000498757.1:n.55+58_55+59insACCCTCCATCCCCTGAGGCTGT
ENST00000389492.3:c.55+58_55+59insACCCTCCATCCCCTGAGGCTGT	ENSP00000374143.3:n.55+58_55+59insACCCTCCATCCCCTGAGGCTGT
ENST00000389494.7:c.55+58_55+59insACCCTCCATCCCCTGAGGCTGT	ENSP00000374145.3:n.55+58_55+59insACCCTCCATCCCCTGAGGCTGT
ENST00000485094.1:n.76+58_76+59insACCCTCCATCCCCTGAGGCTGT
NM_005199.4:c.55+58_55+59insACCCTCCATCCCCTGAGGCTGT	NP_005190.4:n.55+58_55+59insACCCTCCATCCCCTGAGGCTGT
NM_005199.5:c.55+58_55+59insACCCTCCATCCCCTGAGGCTGT MANE Select	NP_005190.4:n.55+58_55+59insACCCTCCATCCCCTGAGGCTGT