Canonical Allele Identifier: CA409636091

Gene: CHRNA4

Linked Data

• gnomAD v4: 20-63350476-A-T
• MyVariant Identifiers: chr20:g.61981828A>T (hg19) ; chr20:g.63350476A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350476A>T , CM000682.2:g.63350476A>T	GRCh38
NC_000020.10:g.61981828A>T , CM000682.1:g.61981828A>T	GRCh37
NC_000020.9:g.61452272A>T	NCBI36
NG_011931.1:g.15868T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.935T>A MANE Select	ENSP00000359285.4:p.Phe312Tyr
ENST00000370263.8:c.935T>A	ENSP00000359285.4:p.Phe312Tyr
ENST00000463705.5:n.1583T>A
ENST00000467563.3:n.1005T>A
ENST00000498043.6:c.959T>A
ENST00000615287.4:c.722T>A	ENSP00000483388.1:p.Phe241Tyr
ENST00000627000.1:c.*624T>A	ENSP00000486914.1:n.*624T>A
ENST00000630240.1:n.656T>A
NM_000744.6:c.935T>A	NP_000735.1:p.Phe312Tyr
NM_001256573.1:c.407T>A	NP_001243502.1:p.Phe136Tyr
NR_046317.1:n.1191T>A
XM_011528524.1:c.722T>A	XP_011526826.1:p.Phe241Tyr
XM_017027625.2:c.407T>A	XP_016883114.1:p.Phe136Tyr
XM_024451822.1:c.407T>A	XP_024307590.1:p.Phe136Tyr
NM_001256573.2:c.407T>A	NP_001243502.1:p.Phe136Tyr
NR_046317.2:n.1144T>A
NM_000744.7:c.935T>A MANE Select	NP_000735.1:p.Phe312Tyr