Canonical Allele Identifier: CA746489672

Gene: CHRNA4

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63346204G>C , CM000682.2:g.63346204G>C	GRCh38
NC_000020.10:g.61977556G>C , CM000682.1:g.61977556G>C	GRCh37
NC_000020.9:g.61448000G>C	NCBI36
NG_011931.1:g.20140C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.*534C>G MANE Select	ENSP00000359285.4:n.*534C>G
ENST00000370263.8:c.*534C>G	ENSP00000359285.4:n.*534C>G
ENST00000463705.5:n.3066C>G
ENST00000615287.4:c.*534C>G	ENSP00000483388.1:n.*534C>G
ENST00000631289.1:n.732C>G
NM_000744.6:c.*534C>G	NP_000735.1:n.*534C>G
NM_001256573.1:c.*534C>G	NP_001243502.1:n.*534C>G
NR_046317.1:n.2674C>G
XM_011528524.1:c.*534C>G	XP_011526826.1:n.*534C>G
XM_017027625.2:c.*534C>G	XP_016883114.1:n.*534C>G
XM_024451822.1:c.*534C>G	XP_024307590.1:n.*534C>G
NM_001256573.2:c.*534C>G	NP_001243502.1:n.*534C>G
NR_046317.2:n.2627C>G
NM_000744.7:c.*534C>G MANE Select	NP_000735.1:n.*534C>G