Canonical Allele Identifier: CA2244610080
Gene: CHRNE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4898402_4898403delinsTA , CM000679.2:g.4898402_4898403delinsTA GRCh38
NC_000017.10:g.4801697_4801698delinsTA , CM000679.1:g.4801697_4801698delinsTA GRCh37
NC_000017.9:g.4742476_4742477delinsTA NCBI36
NG_008029.2:g.9673_9674delinsTA
NG_028005.1:g.70063_70064delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000649488.2:c.*333_*334delinsTA MANE Select ENSP00000497829.1:n.*333_*334delinsTA
ENST00000649830.1:c.*451_*452delinsTA ENSP00000496907.1:n.*451_*452delinsTA
ENST00000652550.1:n.1541_1542delinsTA
ENST00000293780.4:c.*333_*334delinsTA ENSP00000293780.4:n.*333_*334delinsTA
ENST00000572438.1:n.1501_1502delinsTA
NM_000080.3:c.*333_*334delinsTA NP_000071.1:n.*333_*334delinsTA
NM_000080.4:c.*333_*334delinsTA MANE Select NP_000071.1:n.*333_*334delinsTA
XM_017024115.1:c.*333_*334delinsTA XP_016879604.1:n.*333_*334delinsTA