Canonical Allele Identifier: CA409635870

Gene: CHRNA4

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000370263.9:c.970A>T MANE Select	ENSP00000359285.4:p.Thr324Ser
ENST00000370263.8:c.970A>T	ENSP00000359285.4:p.Thr324Ser
ENST00000463705.5:n.1618A>T
ENST00000467563.3:n.1040A>T
ENST00000498043.6:c.994A>T
ENST00000615287.4:c.757A>T	ENSP00000483388.1:p.Thr253Ser
ENST00000627000.1:c.*659A>T	ENSP00000486914.1:n.*659A>T
ENST00000630240.1:n.691A>T
NM_000744.6:c.970A>T	NP_000735.1:p.Thr324Ser
NM_001256573.1:c.442A>T	NP_001243502.1:p.Thr148Ser
NR_046317.1:n.1226A>T
XM_011528524.1:c.757A>T	XP_011526826.1:p.Thr253Ser
XM_017027625.2:c.442A>T	XP_016883114.1:p.Thr148Ser
XM_024451822.1:c.442A>T	XP_024307590.1:p.Thr148Ser
NM_001256573.2:c.442A>T	NP_001243502.1:p.Thr148Ser
NR_046317.2:n.1179A>T
NM_000744.7:c.970A>T MANE Select	NP_000735.1:p.Thr324Ser