Canonical Allele Identifier: CA511339004

Gene: CHRNA4

Linked Data

• gnomAD v4: 20-63350559-C-G
• MyVariant Identifiers: chr20:g.61981911C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350559C>G , CM000682.2:g.63350559C>G	GRCh38
NC_000020.10:g.61981911C>G , CM000682.1:g.61981911C>G	GRCh37
NC_000020.9:g.61452355C>G	NCBI36
NG_011931.1:g.15785G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000370263.9:c.852G>C MANE Select	ENSP00000359285.4:p.Ser284=
ENST00000370263.8:c.852G>C	ENSP00000359285.4:p.Ser284=
ENST00000463705.5:n.1500G>C
ENST00000467563.3:n.922G>C
ENST00000498043.6:c.876G>C
ENST00000615287.4:c.639G>C	ENSP00000483388.1:p.Ser213=
ENST00000627000.1:c.*541G>C	ENSP00000486914.1:n.*541G>C
ENST00000630240.1:n.573G>C
NM_000744.6:c.852G>C	NP_000735.1:p.Ser284=
NM_001256573.1:c.324G>C	NP_001243502.1:p.Ser108=
NR_046317.1:n.1108G>C
XM_011528524.1:c.639G>C	XP_011526826.1:p.Ser213=
XM_017027625.2:c.324G>C	XP_016883114.1:p.Ser108=
XM_024451822.1:c.324G>C	XP_024307590.1:p.Ser108=
NM_001256573.2:c.324G>C	NP_001243502.1:p.Ser108=
NR_046317.2:n.1061G>C
NM_000744.7:c.852G>C MANE Select	NP_000735.1:p.Ser284=