Canonical Allele Identifier: CA409638326

Gene: CHRNA4

Linked Data

• MyVariant Identifiers: chr20:g.61982263A>G (hg19) ; chr20:g.63350911A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350911A>G , CM000682.2:g.63350911A>G	GRCh38
NC_000020.10:g.61982263A>G , CM000682.1:g.61982263A>G	GRCh37
NC_000020.9:g.61452707A>G	NCBI36
NG_011931.1:g.15433T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.500T>C MANE Select	ENSP00000359285.4:p.Phe167Ser
ENST00000370263.8:c.500T>C	ENSP00000359285.4:p.Phe167Ser
ENST00000463705.5:n.1148T>C
ENST00000467563.3:n.570T>C
ENST00000498043.6:c.524T>C
ENST00000615287.4:c.287T>C	ENSP00000483388.1:p.Phe96Ser
ENST00000627000.1:c.*189T>C	ENSP00000486914.1:n.*189T>C
ENST00000628665.1:n.543T>C
ENST00000630240.1:n.221T>C
NM_000744.6:c.500T>C	NP_000735.1:p.Phe167Ser
NM_001256573.1:c.-29T>C	NP_001243502.1:n.-29T>C
NR_046317.1:n.756T>C
XM_011528524.1:c.287T>C	XP_011526826.1:p.Phe96Ser
XM_017027625.2:c.-29T>C	XP_016883114.1:n.-29T>C
XM_024451822.1:c.-29T>C	XP_024307590.1:n.-29T>C
NM_001256573.2:c.-29T>C	NP_001243502.1:n.-29T>C
NR_046317.2:n.709T>C
NM_000744.7:c.500T>C MANE Select	NP_000735.1:p.Phe167Ser