Canonical Allele Identifier: CA409635501

Gene: CHRNA4

Linked Data

• MyVariant Identifiers: chr20:g.61981735C>G (hg19) ; chr20:g.63350383C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350383C>G , CM000682.2:g.63350383C>G	GRCh38
NC_000020.10:g.61981735C>G , CM000682.1:g.61981735C>G	GRCh37
NC_000020.9:g.61452179C>G	NCBI36
NG_011931.1:g.15961G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.1028G>C MANE Select	ENSP00000359285.4:p.Trp343Ser
ENST00000370263.8:c.1028G>C	ENSP00000359285.4:p.Trp343Ser
ENST00000463705.5:n.1676G>C
ENST00000467563.3:n.1098G>C
ENST00000498043.6:c.1052G>C
ENST00000615287.4:c.815G>C	ENSP00000483388.1:p.Trp272Ser
ENST00000627000.1:c.*717G>C	ENSP00000486914.1:n.*717G>C
ENST00000630240.1:n.749G>C
NM_000744.6:c.1028G>C	NP_000735.1:p.Trp343Ser
NM_001256573.1:c.500G>C	NP_001243502.1:p.Trp167Ser
NR_046317.1:n.1284G>C
XM_011528524.1:c.815G>C	XP_011526826.1:p.Trp272Ser
XM_017027625.2:c.500G>C	XP_016883114.1:p.Trp167Ser
XM_024451822.1:c.500G>C	XP_024307590.1:p.Trp167Ser
NM_001256573.2:c.500G>C	NP_001243502.1:p.Trp167Ser
NR_046317.2:n.1237G>C
NM_000744.7:c.1028G>C MANE Select	NP_000735.1:p.Trp343Ser