Canonical Allele Identifier: CA409637309

Gene: CHRNA4

Linked Data

• gnomAD v3: 20-63350757-G-T
• gnomAD v4: 20-63350757-G-T
• MyVariant Identifiers: chr20:g.61982109G>T (hg19) ; chr20:g.63350757G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350757G>T , CM000682.2:g.63350757G>T	GRCh38
NC_000020.10:g.61982109G>T , CM000682.1:g.61982109G>T	GRCh37
NC_000020.9:g.61452553G>T	NCBI36
NG_011931.1:g.15587C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.654C>A MANE Select	ENSP00000359285.4:p.Tyr218Ter
ENST00000370263.8:c.654C>A	ENSP00000359285.4:p.Tyr218Ter
ENST00000463705.5:n.1302C>A
ENST00000467563.3:n.724C>A
ENST00000498043.6:c.678C>A
ENST00000615287.4:c.441C>A	ENSP00000483388.1:p.Tyr147Ter
ENST00000627000.1:c.*343C>A	ENSP00000486914.1:n.*343C>A
ENST00000630240.1:n.375C>A
NM_000744.6:c.654C>A	NP_000735.1:p.Tyr218Ter
NM_001256573.1:c.126C>A	NP_001243502.1:p.Tyr42Ter
NR_046317.1:n.910C>A
XM_011528524.1:c.441C>A	XP_011526826.1:p.Tyr147Ter
XM_017027625.2:c.126C>A	XP_016883114.1:p.Tyr42Ter
XM_024451822.1:c.126C>A	XP_024307590.1:p.Tyr42Ter
NM_001256573.2:c.126C>A	NP_001243502.1:p.Tyr42Ter
NR_046317.2:n.863C>A
NM_000744.7:c.654C>A MANE Select	NP_000735.1:p.Tyr218Ter