Canonical Allele Identifier: CA409638157
Gene: CHRNA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1059852
ClinVar RCV Id: RCV001369211
dbSNP Id: rs2068586748

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63350889G>C , CM000682.2:g.63350889G>C GRCh38
NC_000020.10:g.61982241G>C , CM000682.1:g.61982241G>C GRCh37
NC_000020.9:g.61452685G>C NCBI36
NG_011931.1:g.15455C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370263.9:c.522C>G MANE Select ENSP00000359285.4:p.Asn174Lys
ENST00000370263.8:c.522C>G ENSP00000359285.4:p.Asn174Lys
ENST00000463705.5:n.1170C>G
ENST00000467563.3:n.592C>G
ENST00000498043.6:c.546C>G
ENST00000615287.4:c.309C>G ENSP00000483388.1:p.Asn103Lys
ENST00000627000.1:c.*211C>G ENSP00000486914.1:n.*211C>G
ENST00000630240.1:n.243C>G
NM_000744.6:c.522C>G NP_000735.1:p.Asn174Lys
NM_001256573.1:c.-7C>G NP_001243502.1:n.-7C>G
NR_046317.1:n.778C>G
XM_011528524.1:c.309C>G XP_011526826.1:p.Asn103Lys
XM_017027625.2:c.-7C>G XP_016883114.1:n.-7C>G
XM_024451822.1:c.-7C>G XP_024307590.1:n.-7C>G
NM_001256573.2:c.-7C>G NP_001243502.1:n.-7C>G
NR_046317.2:n.731C>G
NM_000744.7:c.522C>G MANE Select NP_000735.1:p.Asn174Lys