Canonical Allele Identifier: CA1019264382

Gene: CHRNA4

Linked Data

• gnomAD v3: 20-63350744-ACTTCCTGG-A
• gnomAD v4: 20-63350744-ACTTCCTGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350745_63350752del , CM000682.2:g.63350745_63350752del	GRCh38
NC_000020.10:g.61982097_61982104del , CM000682.1:g.61982097_61982104del	GRCh37
NC_000020.9:g.61452541_61452548del	NCBI36
NG_011931.1:g.15592_15599del

Transcript Alleles

HGVS	Amino-acid change
ENST00000370263.9:c.659_666del MANE Select	ENSP00000359285.4:p.Thr220IlefsTer?
ENST00000370263.8:c.659_666del	ENSP00000359285.4:p.Thr220IlefsTer?
ENST00000463705.5:n.1307_1314del
ENST00000467563.3:n.729_736del
ENST00000498043.6:c.683_690del
ENST00000615287.4:c.446_453del	ENSP00000483388.1:p.Thr149IlefsTer?
ENST00000627000.1:c.*348_*355del	ENSP00000486914.1:n.*348_*355del
ENST00000630240.1:n.380_387del
NM_000744.6:c.659_666del	NP_000735.1:p.Thr220IlefsTer?
NM_001256573.1:c.131_138del	NP_001243502.1:p.Thr44IlefsTer?
NR_046317.1:n.915_922del
XM_011528524.1:c.446_453del	XP_011526826.1:p.Thr149IlefsTer?
XM_017027625.2:c.131_138del	XP_016883114.1:p.Thr44IlefsTer?
XM_024451822.1:c.131_138del	XP_024307590.1:p.Thr44IlefsTer?
NM_001256573.2:c.131_138del	NP_001243502.1:p.Thr44IlefsTer?
NR_046317.2:n.868_875del
NM_000744.7:c.659_666del MANE Select	NP_000735.1:p.Thr220IlefsTer?