Canonical Allele Identifier: CA1019264392

Gene: CHRNA4

Linked Data

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

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350744_63350745insT , CM000682.2:g.63350744_63350745insT	GRCh38
NC_000020.10:g.61982096_61982097insT , CM000682.1:g.61982096_61982097insT	GRCh37
NC_000020.9:g.61452540_61452541insT	NCBI36
NG_011931.1:g.15599_15600insA

Transcript Alleles

HGVS	Amino-acid change
ENST00000370263.9:c.666_667insA MANE Select	ENSP00000359285.4:p.Tyr223IlefsTer?
ENST00000370263.8:c.666_667insA	ENSP00000359285.4:p.Tyr223IlefsTer?
ENST00000463705.5:n.1314_1315insA
ENST00000467563.3:n.736_737insA
ENST00000498043.6:c.690_691insA
ENST00000615287.4:c.453_454insA	ENSP00000483388.1:p.Tyr152IlefsTer?
ENST00000627000.1:c.*355_*356insA	ENSP00000486914.1:n.*355_*356insA
ENST00000630240.1:n.387_388insA
NM_000744.6:c.666_667insA	NP_000735.1:p.Tyr223IlefsTer?
NM_001256573.1:c.138_139insA	NP_001243502.1:p.Tyr47IlefsTer?
NR_046317.1:n.922_923insA
XM_011528524.1:c.453_454insA	XP_011526826.1:p.Tyr152IlefsTer?
XM_017027625.2:c.138_139insA	XP_016883114.1:p.Tyr47IlefsTer?
XM_024451822.1:c.138_139insA	XP_024307590.1:p.Tyr47IlefsTer?
NM_001256573.2:c.138_139insA	NP_001243502.1:p.Tyr47IlefsTer?
NR_046317.2:n.875_876insA
NM_000744.7:c.666_667insA MANE Select	NP_000735.1:p.Tyr223IlefsTer?