Canonical Allele Identifier: CA409638116

Gene: CHRNA4

Linked Data

• MyVariant Identifiers: chr20:g.61982231T>G (hg19) ; chr20:g.63350879T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350879T>G , CM000682.2:g.63350879T>G	GRCh38
NC_000020.10:g.61982231T>G , CM000682.1:g.61982231T>G	GRCh37
NC_000020.9:g.61452675T>G	NCBI36
NG_011931.1:g.15465A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.532A>C MANE Select	ENSP00000359285.4:p.Lys178Gln
ENST00000370263.8:c.532A>C	ENSP00000359285.4:p.Lys178Gln
ENST00000463705.5:n.1180A>C
ENST00000467563.3:n.602A>C
ENST00000498043.6:c.556A>C
ENST00000615287.4:c.319A>C	ENSP00000483388.1:p.Lys107Gln
ENST00000627000.1:c.*221A>C	ENSP00000486914.1:n.*221A>C
ENST00000630240.1:n.253A>C
NM_000744.6:c.532A>C	NP_000735.1:p.Lys178Gln
NM_001256573.1:c.4A>C	NP_001243502.1:p.Lys2Gln
NR_046317.1:n.788A>C
XM_011528524.1:c.319A>C	XP_011526826.1:p.Lys107Gln
XM_017027625.2:c.4A>C	XP_016883114.1:p.Lys2Gln
XM_024451822.1:c.4A>C	XP_024307590.1:p.Lys2Gln
NM_001256573.2:c.4A>C	NP_001243502.1:p.Lys2Gln
NR_046317.2:n.741A>C
NM_000744.7:c.532A>C MANE Select	NP_000735.1:p.Lys178Gln