Canonical Allele Identifier: CA511338869

Gene: CHRNA4

Linked Data

• MyVariant Identifiers: chr20:g.61981932C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350580C>G , CM000682.2:g.63350580C>G	GRCh38
NC_000020.10:g.61981932C>G , CM000682.1:g.61981932C>G	GRCh37
NC_000020.9:g.61452376C>G	NCBI36
NG_011931.1:g.15764G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.831G>C MANE Select	ENSP00000359285.4:p.Leu277=
ENST00000370263.8:c.831G>C	ENSP00000359285.4:p.Leu277=
ENST00000463705.5:n.1479G>C
ENST00000467563.3:n.901G>C
ENST00000498043.6:c.855G>C
ENST00000615287.4:c.618G>C	ENSP00000483388.1:p.Leu206=
ENST00000627000.1:c.*520G>C	ENSP00000486914.1:n.*520G>C
ENST00000630240.1:n.552G>C
NM_000744.6:c.831G>C	NP_000735.1:p.Leu277=
NM_001256573.1:c.303G>C	NP_001243502.1:p.Leu101=
NR_046317.1:n.1087G>C
XM_011528524.1:c.618G>C	XP_011526826.1:p.Leu206=
XM_017027625.2:c.303G>C	XP_016883114.1:p.Leu101=
XM_024451822.1:c.303G>C	XP_024307590.1:p.Leu101=
NM_001256573.2:c.303G>C	NP_001243502.1:p.Leu101=
NR_046317.2:n.1040G>C
NM_000744.7:c.831G>C MANE Select	NP_000735.1:p.Leu277=