Canonical Allele Identifier: CA2244610266
Gene: CHRNE HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4898687_4898703delinsAAAATCAATTTCCTACT , CM000679.2:g.4898687_4898703delinsAAAATCAATTTCCTACT GRCh38
NC_000017.10:g.4801982_4801998delinsAAAATCAATTTCCTACT , CM000679.1:g.4801982_4801998delinsAAAATCAATTTCCTACT GRCh37
NC_000017.9:g.4742761_4742777delinsAAAATCAATTTCCTACT NCBI36
NG_008029.2:g.9373_9389delinsAGTAGGAAATTGATTTT
NG_028005.1:g.70348_70364delinsAAAATCAATTTCCTACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000649488.2:c.*33_*49delinsAGTAGGAAATTGATTTT MANE Select ENSP00000497829.1:n.*33_*49delinsAGTAGGAAATTGATTTT
ENST00000649830.1:c.*151_*167delinsAGTAGGAAATTGATTTT ENSP00000496907.1:n.*151_*167delinsAGTAGGAAATTGATTTT
ENST00000652550.1:n.1241_1257delinsAGTAGGAAATTGATTTT
ENST00000293780.4:c.*33_*49delinsAGTAGGAAATTGATTTT ENSP00000293780.4:n.*33_*49delinsAGTAGGAAATTGATTTT
ENST00000572438.1:n.1201_1217delinsAGTAGGAAATTGATTTT
NM_000080.3:c.*33_*49delinsAGTAGGAAATTGATTTT NP_000071.1:n.*33_*49delinsAGTAGGAAATTGATTTT
NM_000080.4:c.*33_*49delinsAGTAGGAAATTGATTTT MANE Select NP_000071.1:n.*33_*49delinsAGTAGGAAATTGATTTT
XM_017024115.1:c.*33_*49delinsAGTAGGAAATTGATTTT XP_016879604.1:n.*33_*49delinsAGTAGGAAATTGATTTT
Search 100 bp 5'
Search 100 bp 3'