Canonical Allele Identifier: CA409637861

Gene: CHRNA4

Linked Data

• MyVariant Identifiers: chr20:g.61982194T>A (hg19) ; chr20:g.63350842T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350842T>A , CM000682.2:g.63350842T>A	GRCh38
NC_000020.10:g.61982194T>A , CM000682.1:g.61982194T>A	GRCh37
NC_000020.9:g.61452638T>A	NCBI36
NG_011931.1:g.15502A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.569A>T MANE Select	ENSP00000359285.4:p.Asp190Val
ENST00000370263.8:c.569A>T	ENSP00000359285.4:p.Asp190Val
ENST00000463705.5:n.1217A>T
ENST00000467563.3:n.639A>T
ENST00000498043.6:c.593A>T
ENST00000615287.4:c.356A>T	ENSP00000483388.1:p.Asp119Val
ENST00000627000.1:c.*258A>T	ENSP00000486914.1:n.*258A>T
ENST00000630240.1:n.290A>T
NM_000744.6:c.569A>T	NP_000735.1:p.Asp190Val
NM_001256573.1:c.41A>T	NP_001243502.1:p.Asp14Val
NR_046317.1:n.825A>T
XM_011528524.1:c.356A>T	XP_011526826.1:p.Asp119Val
XM_017027625.2:c.41A>T	XP_016883114.1:p.Asp14Val
XM_024451822.1:c.41A>T	XP_024307590.1:p.Asp14Val
NM_001256573.2:c.41A>T	NP_001243502.1:p.Asp14Val
NR_046317.2:n.778A>T
NM_000744.7:c.569A>T MANE Select	NP_000735.1:p.Asp190Val