Canonical Allele Identifier: CA409635515

Gene: CHRNA4

Linked Data

• MyVariant Identifiers: chr20:g.61981738G>T (hg19) ; chr20:g.63350386G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350386G>T , CM000682.2:g.63350386G>T	GRCh38
NC_000020.10:g.61981738G>T , CM000682.1:g.61981738G>T	GRCh37
NC_000020.9:g.61452182G>T	NCBI36
NG_011931.1:g.15958C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.1025C>A MANE Select	ENSP00000359285.4:p.Thr342Asn
ENST00000370263.8:c.1025C>A	ENSP00000359285.4:p.Thr342Asn
ENST00000463705.5:n.1673C>A
ENST00000467563.3:n.1095C>A
ENST00000498043.6:c.1049C>A
ENST00000615287.4:c.812C>A	ENSP00000483388.1:p.Thr271Asn
ENST00000627000.1:c.*714C>A	ENSP00000486914.1:n.*714C>A
ENST00000630240.1:n.746C>A
NM_000744.6:c.1025C>A	NP_000735.1:p.Thr342Asn
NM_001256573.1:c.497C>A	NP_001243502.1:p.Thr166Asn
NR_046317.1:n.1281C>A
XM_011528524.1:c.812C>A	XP_011526826.1:p.Thr271Asn
XM_017027625.2:c.497C>A	XP_016883114.1:p.Thr166Asn
XM_024451822.1:c.497C>A	XP_024307590.1:p.Thr166Asn
NM_001256573.2:c.497C>A	NP_001243502.1:p.Thr166Asn
NR_046317.2:n.1234C>A
NM_000744.7:c.1025C>A MANE Select	NP_000735.1:p.Thr342Asn