Canonical Allele Identifier: CA2577452934

Gene: CHRNA4

Linked Data

• gnomAD v4: 20-63350462-CGAA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350465_63350467del , CM000682.2:g.63350465_63350467del	GRCh38
NC_000020.10:g.61981817_61981819del , CM000682.1:g.61981817_61981819del	GRCh37
NC_000020.9:g.61452261_61452263del	NCBI36
NG_011931.1:g.15879_15881del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.946_948del MANE Select	ENSP00000359285.4:p.Phe316del
ENST00000370263.8:c.946_948del	ENSP00000359285.4:p.Phe316del
ENST00000463705.5:n.1594_1596del
ENST00000467563.3:n.1016_1018del
ENST00000498043.6:c.970_972del
ENST00000615287.4:c.733_735del	ENSP00000483388.1:p.Phe245del
ENST00000627000.1:c.*635_*637del	ENSP00000486914.1:n.*635_*637del
ENST00000630240.1:n.667_669del
NM_000744.6:c.946_948del	NP_000735.1:p.Phe316del
NM_001256573.1:c.418_420del	NP_001243502.1:p.Phe140del
NR_046317.1:n.1202_1204del
XM_011528524.1:c.733_735del	XP_011526826.1:p.Phe245del
XM_017027625.2:c.418_420del	XP_016883114.1:p.Phe140del
XM_024451822.1:c.418_420del	XP_024307590.1:p.Phe140del
NM_001256573.2:c.418_420del	NP_001243502.1:p.Phe140del
NR_046317.2:n.1155_1157del
NM_000744.7:c.946_948del MANE Select	NP_000735.1:p.Phe316del