Canonical Allele Identifier: CA409637390

Gene: CHRNA4

Linked Data

• MyVariant Identifiers: chr20:g.61982122G>T (hg19) ; chr20:g.63350770G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350770G>T , CM000682.2:g.63350770G>T	GRCh38
NC_000020.10:g.61982122G>T , CM000682.1:g.61982122G>T	GRCh37
NC_000020.9:g.61452566G>T	NCBI36
NG_011931.1:g.15574C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.641C>A MANE Select	ENSP00000359285.4:p.Ala214Asp
ENST00000370263.8:c.641C>A	ENSP00000359285.4:p.Ala214Asp
ENST00000463705.5:n.1289C>A
ENST00000467563.3:n.711C>A
ENST00000498043.6:c.665C>A
ENST00000615287.4:c.428C>A	ENSP00000483388.1:p.Ala143Asp
ENST00000627000.1:c.*330C>A	ENSP00000486914.1:n.*330C>A
ENST00000630240.1:n.362C>A
NM_000744.6:c.641C>A	NP_000735.1:p.Ala214Asp
NM_001256573.1:c.113C>A	NP_001243502.1:p.Ala38Asp
NR_046317.1:n.897C>A
XM_011528524.1:c.428C>A	XP_011526826.1:p.Ala143Asp
XM_017027625.2:c.113C>A	XP_016883114.1:p.Ala38Asp
XM_024451822.1:c.113C>A	XP_024307590.1:p.Ala38Asp
NM_001256573.2:c.113C>A	NP_001243502.1:p.Ala38Asp
NR_046317.2:n.850C>A
NM_000744.7:c.641C>A MANE Select	NP_000735.1:p.Ala214Asp