Canonical Allele Identifier: CA2374743222
Gene: CHRNA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63350901_63350915delinsGAAGGGGAAGAAGGT , CM000682.2:g.63350901_63350915delinsGAAGGGGAAGAAGGT GRCh38
NC_000020.10:g.61982253_61982267delinsGAAGGGGAAGAAGGT , CM000682.1:g.61982253_61982267delinsGAAGGGGAAGAAGGT GRCh37
NC_000020.9:g.61452697_61452711delinsGAAGGGGAAGAAGGT NCBI36
NG_011931.1:g.15429_15443delinsACCTTCTTCCCCTTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000370263.9:c.496_510delinsACCTTCTTCCCCTTC MANE Select ENSP00000359285.4:p.Thr166=
ENST00000370263.8:c.496_510delinsACCTTCTTCCCCTTC ENSP00000359285.4:p.Thr166=
ENST00000463705.5:n.1144_1158delinsACCTTCTTCCCCTTC
ENST00000467563.3:n.566_580delinsACCTTCTTCCCCTTC
ENST00000498043.6:c.520_534delinsACCTTCTTCCCCTTC
ENST00000615287.4:c.283_297delinsACCTTCTTCCCCTTC ENSP00000483388.1:p.Thr95=
ENST00000627000.1:c.*185_*199delinsACCTTCTTCCCCTTC ENSP00000486914.1:n.*185_*199delinsACCTTCTTCCCCTTC
ENST00000630240.1:n.217_231delinsACCTTCTTCCCCTTC
NM_000744.6:c.496_510delinsACCTTCTTCCCCTTC NP_000735.1:p.Thr166=
NM_001256573.1:c.-33_-19delinsACCTTCTTCCCCTTC NP_001243502.1:n.-33_-19delinsACCTTCTTCCCCTTC
NR_046317.1:n.752_766delinsACCTTCTTCCCCTTC
XM_011528524.1:c.283_297delinsACCTTCTTCCCCTTC XP_011526826.1:p.Thr95=
XM_017027625.2:c.-33_-19delinsACCTTCTTCCCCTTC XP_016883114.1:n.-33_-19delinsACCTTCTTCCCCTTC
XM_024451822.1:c.-33_-19delinsACCTTCTTCCCCTTC XP_024307590.1:n.-33_-19delinsACCTTCTTCCCCTTC
NM_001256573.2:c.-33_-19delinsACCTTCTTCCCCTTC NP_001243502.1:n.-33_-19delinsACCTTCTTCCCCTTC
NR_046317.2:n.705_719delinsACCTTCTTCCCCTTC
NM_000744.7:c.496_510delinsACCTTCTTCCCCTTC MANE Select NP_000735.1:p.Thr166=