Canonical Allele Identifier: CA1335312158
Gene: CHRNG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232539768_232539777delinsGCTGCTCCTC , CM000664.2:g.232539768_232539777delinsGCTGCTCCTC GRCh38
NC_000002.11:g.233404478_233404487delinsGCTGCTCCTC , CM000664.1:g.233404478_233404487delinsGCTGCTCCTC GRCh37
NC_000002.10:g.233112722_233112731delinsGCTGCTCCTC NCBI36
NG_012954.1:g.5042_5051delinsGCTGCTCCTC
NG_012954.2:g.5077_5086delinsGCTGCTCCTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000651502.1:c.21_30delinsGCTGCTCCTC MANE Select ENSP00000498757.1:p.Pro7=
ENST00000389492.3:c.21_30delinsGCTGCTCCTC ENSP00000374143.3:p.Pro7=
ENST00000389494.7:c.21_30delinsGCTGCTCCTC ENSP00000374145.3:p.Pro7=
ENST00000485094.1:n.42_51delinsGCTGCTCCTC
NM_005199.4:c.21_30delinsGCTGCTCCTC NP_005190.4:p.Pro7=
NM_005199.5:c.21_30delinsGCTGCTCCTC MANE Select NP_005190.4:p.Pro7=
Search 100 bp 5'
Search 100 bp 3'