Canonical Allele Identifier: CA2374747233

Gene: CHRNA4

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63356709G>C , CM000682.2:g.63356709G>C	GRCh38
NC_000020.10:g.61988061G>C , CM000682.1:g.61988061G>C	GRCh37
NC_000020.9:g.61458505G>C	NCBI36
NG_011931.1:g.9635C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.229-294C>G MANE Select	ENSP00000359285.4:n.229-294C>G
ENST00000636481.1:n.37-171C>G
ENST00000636726.1:n.34-105C>G
ENST00000675470.1:c.229-294C>G	ENSP00000502096.1:n.229-294C>G
ENST00000370263.8:c.229-294C>G	ENSP00000359285.4:n.229-294C>G
ENST00000463705.5:n.1032-5682C>G
ENST00000467563.3:n.281-294C>G
ENST00000498043.6:c.153-294C>G
ENST00000615287.4:c.-85-294C>G	ENSP00000483388.1:n.-85-294C>G
ENST00000627000.1:c.229-294C>G	ENSP00000486914.1:n.229-294C>G
ENST00000628665.1:n.254-294C>G
NM_000744.6:c.229-294C>G	NP_000735.1:n.229-294C>G
NM_001256573.1:c.-318-294C>G	NP_001243502.1:n.-318-294C>G
NR_046317.1:n.460-294C>G
XM_017027625.2:c.-318-294C>G	XP_016883114.1:n.-318-294C>G
NM_001256573.2:c.-318-294C>G	NP_001243502.1:n.-318-294C>G
NR_046317.2:n.413-294C>G
NM_000744.7:c.229-294C>G MANE Select	NP_000735.1:n.229-294C>G