Canonical Allele Identifier: CA2653785030

Gene: CHRNA4

Linked Data

• gnomAD v4: 20-63350865-CCAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350866_63350868del , CM000682.2:g.63350866_63350868del	GRCh38
NC_000020.10:g.61982218_61982220del , CM000682.1:g.61982218_61982220del	GRCh37
NC_000020.9:g.61452662_61452664del	NCBI36
NG_011931.1:g.15476_15478del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.543_545del MANE Select	ENSP00000359285.4:p.Trp182del
ENST00000370263.8:c.543_545del	ENSP00000359285.4:p.Trp182del
ENST00000463705.5:n.1191_1193del
ENST00000467563.3:n.613_615del
ENST00000498043.6:c.567_569del
ENST00000615287.4:c.330_332del	ENSP00000483388.1:p.Trp111del
ENST00000627000.1:c.*232_*234del	ENSP00000486914.1:n.*232_*234del
ENST00000630240.1:n.264_266del
NM_000744.6:c.543_545del	NP_000735.1:p.Trp182del
NM_001256573.1:c.15_17del	NP_001243502.1:p.Trp6del
NR_046317.1:n.799_801del
XM_011528524.1:c.330_332del	XP_011526826.1:p.Trp111del
XM_017027625.2:c.15_17del	XP_016883114.1:p.Trp6del
XM_024451822.1:c.15_17del	XP_024307590.1:p.Trp6del
NM_001256573.2:c.15_17del	NP_001243502.1:p.Trp6del
NR_046317.2:n.752_754del
NM_000744.7:c.543_545del MANE Select	NP_000735.1:p.Trp182del