Canonical Allele Identifier: CA317431653

Gene: CHRNA4

Linked Data

• dbSNP Id: rs890168894
• gnomAD v3: 20-63349745-G-A
• gnomAD v4: 20-63349745-G-A
• MyVariant Identifiers: chr20:g.61981097G>A (hg19) ; chr20:g.63349745G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63349745G>A , CM000682.2:g.63349745G>A	GRCh38
NC_000020.10:g.61981097G>A , CM000682.1:g.61981097G>A	GRCh37
NC_000020.9:g.61451541G>A	NCBI36
NG_011931.1:g.16599C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.1666C>T MANE Select	ENSP00000359285.4:p.Pro556Ser
ENST00000370263.8:c.1666C>T	ENSP00000359285.4:p.Pro556Ser
ENST00000463705.5:n.2314C>T
ENST00000467563.3:n.1736C>T
ENST00000498043.6:c.1690C>T
ENST00000615287.4:c.1453C>T	ENSP00000483388.1:p.Pro485Ser
ENST00000627000.1:c.*1355C>T	ENSP00000486914.1:n.*1355C>T
ENST00000630240.1:n.1387C>T
NM_000744.6:c.1666C>T	NP_000735.1:p.Pro556Ser
NM_001256573.1:c.1138C>T	NP_001243502.1:p.Pro380Ser
NR_046317.1:n.1922C>T
XM_011528524.1:c.1453C>T	XP_011526826.1:p.Pro485Ser
XM_017027625.2:c.1138C>T	XP_016883114.1:p.Pro380Ser
XM_024451822.1:c.1138C>T	XP_024307590.1:p.Pro380Ser
NM_001256573.2:c.1138C>T	NP_001243502.1:p.Pro380Ser
NR_046317.2:n.1875C>T
NM_000744.7:c.1666C>T MANE Select	NP_000735.1:p.Pro556Ser