Canonical Allele Identifier: CA636613625

Gene: CHRNA4

Linked Data

• dbSNP Id: rs1568810181
• gnomAD v2: 20-61981975-AGCACG-A
• gnomAD v4: 20-63350623-AGCACG-A
• MyVariant Identifiers: chr20:g.61981976_61981980del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350625_63350629del , CM000682.2:g.63350625_63350629del	GRCh38
NC_000020.10:g.61981977_61981981del , CM000682.1:g.61981977_61981981del	GRCh37
NC_000020.9:g.61452421_61452425del	NCBI36
NG_011931.1:g.15716_15720del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.783_787del MANE Select	ENSP00000359285.4:p.Val262GlyfsTer?
ENST00000370263.8:c.783_787del	ENSP00000359285.4:p.Val262GlyfsTer?
ENST00000463705.5:n.1431_1435del
ENST00000467563.3:n.853_857del
ENST00000498043.6:c.807_811del
ENST00000615287.4:c.570_574del	ENSP00000483388.1:p.Val191GlyfsTer?
ENST00000627000.1:c.*472_*476del	ENSP00000486914.1:n.*472_*476del
ENST00000630240.1:n.504_508del
NM_000744.6:c.783_787del	NP_000735.1:p.Val262GlyfsTer?
NM_001256573.1:c.255_259del	NP_001243502.1:p.Val86GlyfsTer?
NR_046317.1:n.1039_1043del
XM_011528524.1:c.570_574del	XP_011526826.1:p.Val191GlyfsTer?
XM_017027625.2:c.255_259del	XP_016883114.1:p.Val86GlyfsTer?
XM_024451822.1:c.255_259del	XP_024307590.1:p.Val86GlyfsTer?
NM_001256573.2:c.255_259del	NP_001243502.1:p.Val86GlyfsTer?
NR_046317.2:n.992_996del
NM_000744.7:c.783_787del MANE Select	NP_000735.1:p.Val262GlyfsTer?