Canonical Allele Identifier: CA2595907716

Gene: CHRNA4

Linked Data

• gnomAD v3: 20-63350750-TGGTG-T
• gnomAD v4: 20-63350750-TGGTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350751_63350754del , CM000682.2:g.63350751_63350754del	GRCh38
NC_000020.10:g.61982103_61982106del , CM000682.1:g.61982103_61982106del	GRCh37
NC_000020.9:g.61452547_61452550del	NCBI36
NG_011931.1:g.15590_15593del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.657_660del MANE Select	ENSP00000359285.4:p.Asn219LysfsTer?
ENST00000370263.8:c.657_660del	ENSP00000359285.4:p.Asn219LysfsTer?
ENST00000463705.5:n.1305_1308del
ENST00000467563.3:n.727_730del
ENST00000498043.6:c.681_684del
ENST00000615287.4:c.444_447del	ENSP00000483388.1:p.Asn148LysfsTer?
ENST00000627000.1:c.*346_*349del	ENSP00000486914.1:n.*346_*349del
ENST00000630240.1:n.378_381del
NM_000744.6:c.657_660del	NP_000735.1:p.Asn219LysfsTer?
NM_001256573.1:c.129_132del	NP_001243502.1:p.Asn43LysfsTer?
NR_046317.1:n.913_916del
XM_011528524.1:c.444_447del	XP_011526826.1:p.Asn148LysfsTer?
XM_017027625.2:c.129_132del	XP_016883114.1:p.Asn43LysfsTer?
XM_024451822.1:c.129_132del	XP_024307590.1:p.Asn43LysfsTer?
NM_001256573.2:c.129_132del	NP_001243502.1:p.Asn43LysfsTer?
NR_046317.2:n.866_869del
NM_000744.7:c.657_660del MANE Select	NP_000735.1:p.Asn219LysfsTer?