Canonical Allele Identifier: CA2842938878

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63349619dup , CM000682.2:g.63349619dup	GRCh38
NC_000020.10:g.61980971dup , CM000682.1:g.61980971dup	GRCh37
NC_000020.9:g.61451415dup	NCBI36
NG_011931.1:g.16725dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.1758+34dup MANE Select	ENSP00000359285.4:n.1758+34dup
ENST00000370263.8:c.1758+34dup	ENSP00000359285.4:n.1758+34dup
ENST00000463705.5:n.2406+34dup
ENST00000467563.3:n.1828+34dup
ENST00000498043.6:c.1782+34dup
ENST00000615287.4:c.1545+34dup	ENSP00000483388.1:n.1545+34dup
ENST00000627000.1:c.*1447+34dup	ENSP00000486914.1:n.*1447+34dup
ENST00000630240.1:n.1513dup
NM_000744.6:c.1758+34dup	NP_000735.1:n.1758+34dup
NM_001256573.1:c.1230+34dup	NP_001243502.1:n.1230+34dup
NR_046317.1:n.2014+34dup
XM_011528524.1:c.1545+34dup	XP_011526826.1:n.1545+34dup
XM_017027625.2:c.1230+34dup	XP_016883114.1:n.1230+34dup
XM_024451822.1:c.1230+34dup	XP_024307590.1:n.1230+34dup
NM_001256573.2:c.1230+34dup	NP_001243502.1:n.1230+34dup
NR_046317.2:n.1967+34dup
NM_000744.7:c.1758+34dup MANE Select	NP_000735.1:n.1758+34dup