Canonical Allele Identifier: CA409635873

Gene: CHRNA4

Linked Data

• COSMIC: COSM6160777
• MyVariant Identifiers: chr20:g.61981793T>C (hg19) ; chr20:g.63350441T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350441T>C , CM000682.2:g.63350441T>C	GRCh38
NC_000020.10:g.61981793T>C , CM000682.1:g.61981793T>C	GRCh37
NC_000020.9:g.61452237T>C	NCBI36
NG_011931.1:g.15903A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000370263.9:c.970A>G MANE Select	ENSP00000359285.4:p.Thr324Ala
ENST00000370263.8:c.970A>G	ENSP00000359285.4:p.Thr324Ala
ENST00000463705.5:n.1618A>G
ENST00000467563.3:n.1040A>G
ENST00000498043.6:c.994A>G
ENST00000615287.4:c.757A>G	ENSP00000483388.1:p.Thr253Ala
ENST00000627000.1:c.*659A>G	ENSP00000486914.1:n.*659A>G
ENST00000630240.1:n.691A>G
NM_000744.6:c.970A>G	NP_000735.1:p.Thr324Ala
NM_001256573.1:c.442A>G	NP_001243502.1:p.Thr148Ala
NR_046317.1:n.1226A>G
XM_011528524.1:c.757A>G	XP_011526826.1:p.Thr253Ala
XM_017027625.2:c.442A>G	XP_016883114.1:p.Thr148Ala
XM_024451822.1:c.442A>G	XP_024307590.1:p.Thr148Ala
NM_001256573.2:c.442A>G	NP_001243502.1:p.Thr148Ala
NR_046317.2:n.1179A>G
NM_000744.7:c.970A>G MANE Select	NP_000735.1:p.Thr324Ala