Canonical Allele Identifier: CA409637975

Gene: CHRNA4

Linked Data

• MyVariant Identifiers: chr20:g.61982209T>A (hg19) ; chr20:g.63350857T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350857T>A , CM000682.2:g.63350857T>A	GRCh38
NC_000020.10:g.61982209T>A , CM000682.1:g.61982209T>A	GRCh37
NC_000020.9:g.61452653T>A	NCBI36
NG_011931.1:g.15487A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.554A>T MANE Select	ENSP00000359285.4:p.Asp185Val
ENST00000370263.8:c.554A>T	ENSP00000359285.4:p.Asp185Val
ENST00000463705.5:n.1202A>T
ENST00000467563.3:n.624A>T
ENST00000498043.6:c.578A>T
ENST00000615287.4:c.341A>T	ENSP00000483388.1:p.Asp114Val
ENST00000627000.1:c.*243A>T	ENSP00000486914.1:n.*243A>T
ENST00000630240.1:n.275A>T
NM_000744.6:c.554A>T	NP_000735.1:p.Asp185Val
NM_001256573.1:c.26A>T	NP_001243502.1:p.Asp9Val
NR_046317.1:n.810A>T
XM_011528524.1:c.341A>T	XP_011526826.1:p.Asp114Val
XM_017027625.2:c.26A>T	XP_016883114.1:p.Asp9Val
XM_024451822.1:c.26A>T	XP_024307590.1:p.Asp9Val
NM_001256573.2:c.26A>T	NP_001243502.1:p.Asp9Val
NR_046317.2:n.763A>T
NM_000744.7:c.554A>T MANE Select	NP_000735.1:p.Asp185Val