Canonical Allele Identifier: CA2244610267
Gene: CHRNE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4898687_4898737delinsAAAATCAATTTCCTACTGGAGATGGGTGGGAAATTGAAGTCGGTGCGAGCT , CM000679.2:g.4898687_4898737delinsAAAATCAATTTCCTACTGGAGATGGGTGGGAAATTGAAGTCGGTGCGAGCT GRCh38
NC_000017.10:g.4801982_4802032delinsAAAATCAATTTCCTACTGGAGATGGGTGGGAAATTGAAGTCGGTGCGAGCT , CM000679.1:g.4801982_4802032delinsAAAATCAATTTCCTACTGGAGATGGGTGGGAAATTGAAGTCGGTGCGAGCT GRCh37
NC_000017.9:g.4742761_4742811delinsAAAATCAATTTCCTACTGGAGATGGGTGGGAAATTGAAGTCGGTGCGAGCT NCBI36
NG_008029.2:g.9339_9389delinsAGCTCGCACCGACTTCAATTTCCCACCCATCTCCAGTAGGAAATTGATTTT
NG_028005.1:g.70348_70398delinsAAAATCAATTTCCTACTGGAGATGGGTGGGAAATTGAAGTCGGTGCGAGCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000649488.2:c.1481_*49delinsAGCTCGCACCGACTTCAATTTCCCACCCATCTCCAGTAGGAAATTGATTTT MANE Select ENSP00000497829.1:n.[c.1481_*49delinsAGCTCGCACCGACTTCAATTTCCC...
ENST00000649830.1:c.*117_*167delinsAGCTCGCACCGACTTCAATTTCCCACCCATCTCCAGTAGGAAATTGATTTT ENSP00000496907.1:n.*117_*167delinsAGCTCGCACCGACTTCAATTTCCCAC...
ENST00000652550.1:n.1207_1257delinsAGCTCGCACCGACTTCAATTTCCCACCCATCTCCAGTAGGAAATTGATTTT
ENST00000293780.4:c.1481_*49delinsAGCTCGCACCGACTTCAATTTCCCACCCATCTCCAGTAGGAAATTGATTTT ENSP00000293780.4:n.[c.1481_*49delinsAGCTCGCACCGACTTCAATTTCCC...
ENST00000572438.1:n.1167_1217delinsAGCTCGCACCGACTTCAATTTCCCACCCATCTCCAGTAGGAAATTGATTTT
NM_000080.3:c.1481_*49delinsAGCTCGCACCGACTTCAATTTCCCACCCATCTCCAGTAGGAAATTGATTTT NP_000071.1:n.[c.1481_*49delinsAGCTCGCACCGACTTCAATTTCCCACCCAT...
NM_000080.4:c.1481_*49delinsAGCTCGCACCGACTTCAATTTCCCACCCATCTCCAGTAGGAAATTGATTTT MANE Select NP_000071.1:n.[c.1481_*49delinsAGCTCGCACCGACTTCAATTTCCCACCCAT...
XM_017024115.1:c.1445_*49delinsAGCTCGCACCGACTTCAATTTCCCACCCATCTCCAGTAGGAAATTGATTTT XP_016879604.1:n.[c.1445_*49delinsAGCTCGCACCGACTTCAATTTCCCACC...