Canonical Allele Identifier: CA1019264368

Gene: CHRNA4

Linked Data

• gnomAD v3: 20-63350743-TAC-T
• gnomAD v4: 20-63350743-TAC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350744_63350745del , CM000682.2:g.63350744_63350745del	GRCh38
NC_000020.10:g.61982096_61982097del , CM000682.1:g.61982096_61982097del	GRCh37
NC_000020.9:g.61452540_61452541del	NCBI36
NG_011931.1:g.15599_15600del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.666_667del MANE Select	ENSP00000359285.4:p.Tyr223ArgfsTer?
ENST00000370263.8:c.666_667del	ENSP00000359285.4:p.Tyr223ArgfsTer?
ENST00000463705.5:n.1314_1315del
ENST00000467563.3:n.736_737del
ENST00000498043.6:c.690_691del
ENST00000615287.4:c.453_454del	ENSP00000483388.1:p.Tyr152ArgfsTer?
ENST00000627000.1:c.*355_*356del	ENSP00000486914.1:n.*355_*356del
ENST00000630240.1:n.387_388del
NM_000744.6:c.666_667del	NP_000735.1:p.Tyr223ArgfsTer?
NM_001256573.1:c.138_139del	NP_001243502.1:p.Tyr47ArgfsTer?
NR_046317.1:n.922_923del
XM_011528524.1:c.453_454del	XP_011526826.1:p.Tyr152ArgfsTer?
XM_017027625.2:c.138_139del	XP_016883114.1:p.Tyr47ArgfsTer?
XM_024451822.1:c.138_139del	XP_024307590.1:p.Tyr47ArgfsTer?
NM_001256573.2:c.138_139del	NP_001243502.1:p.Tyr47ArgfsTer?
NR_046317.2:n.875_876del
NM_000744.7:c.666_667del MANE Select	NP_000735.1:p.Tyr223ArgfsTer?