Canonical Allele Identifier: CA2244610218
Gene: CHRNE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4898629_4898633delinsAGATT , CM000679.2:g.4898629_4898633delinsAGATT GRCh38
NC_000017.10:g.4801924_4801928delinsAGATT , CM000679.1:g.4801924_4801928delinsAGATT GRCh37
NC_000017.9:g.4742703_4742707delinsAGATT NCBI36
NG_008029.2:g.9443_9447delinsAATCT
NG_028005.1:g.70290_70294delinsAGATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000649488.2:c.*103_*107delinsAATCT MANE Select ENSP00000497829.1:n.*103_*107delinsAATCT
ENST00000649830.1:c.*221_*225delinsAATCT ENSP00000496907.1:n.*221_*225delinsAATCT
ENST00000652550.1:n.1311_1315delinsAATCT
ENST00000293780.4:c.*103_*107delinsAATCT ENSP00000293780.4:n.*103_*107delinsAATCT
ENST00000572438.1:n.1271_1275delinsAATCT
NM_000080.3:c.*103_*107delinsAATCT NP_000071.1:n.*103_*107delinsAATCT
NM_000080.4:c.*103_*107delinsAATCT MANE Select NP_000071.1:n.*103_*107delinsAATCT
XM_017024115.1:c.*103_*107delinsAATCT XP_016879604.1:n.*103_*107delinsAATCT