Canonical Allele Identifier: CA2244610196
Gene: CHRNE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4898598_4898599delinsAC , CM000679.2:g.4898598_4898599delinsAC GRCh38
NC_000017.10:g.4801893_4801894delinsAC , CM000679.1:g.4801893_4801894delinsAC GRCh37
NC_000017.9:g.4742672_4742673delinsAC NCBI36
NG_008029.2:g.9477_9478delinsGT
NG_028005.1:g.70259_70260delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000649488.2:c.*137_*138delinsGT MANE Select ENSP00000497829.1:n.*137_*138delinsGT
ENST00000649830.1:c.*255_*256delinsGT ENSP00000496907.1:n.*255_*256delinsGT
ENST00000652550.1:n.1345_1346delinsGT
ENST00000293780.4:c.*137_*138delinsGT ENSP00000293780.4:n.*137_*138delinsGT
ENST00000572438.1:n.1305_1306delinsGT
NM_000080.3:c.*137_*138delinsGT NP_000071.1:n.*137_*138delinsGT
NM_000080.4:c.*137_*138delinsGT MANE Select NP_000071.1:n.*137_*138delinsGT
XM_017024115.1:c.*137_*138delinsGT XP_016879604.1:n.*137_*138delinsGT