Canonical Allele Identifier: CA1308865693
Gene: CHN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.174824450C= , CM000664.2:g.174824450C= GRCh38
NC_000002.11:g.175689178C= , CM000664.1:g.175689178C= GRCh37
NC_000002.10:g.175397424C= NCBI36
NG_012642.1:g.185993G=
NG_012642.2:g.185993G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295497.13:c.321G= ENSP00000295497.7:p.Gln107=
ENST00000444394.7:c.321G= ENSP00000411911.2:p.Gln107=
ENST00000295497.12:c.321G= ENSP00000295497.7:p.Gln107=
ENST00000409089.7:c.21G= ENSP00000386322.3:p.Gln7=
ENST00000409900.9:c.696G= MANE Select ENSP00000386741.4:p.Gln232=
ENST00000413882.6:c.150G= ENSP00000410496.2:p.Gln50=
ENST00000425395.6:c.*143G= ENSP00000405270.2:n.*143G=
ENST00000443238.6:c.174G= ENSP00000409798.2:p.Gln58=
ENST00000444394.6:c.321G= ENSP00000411911.2:p.Gln107=
ENST00000444573.2:c.540G= ENSP00000392603.2:p.Gln180=
ENST00000488080.6:n.339G=
ENST00000650731.1:c.21G= ENSP00000499146.1:p.Gln7=
ENST00000650938.1:c.220G=
ENST00000651246.1:c.288G= ENSP00000498484.1:p.Gln96=
ENST00000651373.1:c.210G= ENSP00000499174.1:p.Gln70=
ENST00000651501.1:c.*143G= ENSP00000498894.1:n.*143G=
ENST00000651717.1:c.253-11968G= ENSP00000499124.1:n.253-11968G=
ENST00000652036.1:c.321G= ENSP00000499139.1:p.Gln107=
ENST00000652154.1:n.594G=
ENST00000295497.11:c.321G= ENSP00000295497.7:p.Gln107=
ENST00000409089.6:c.21G= ENSP00000386322.2:p.Gln7=
ENST00000409156.7:c.618G= ENSP00000386470.3:p.Gln206=
ENST00000409597.5:c.144G= ENSP00000386469.1:p.Gln48=
ENST00000409900.7:c.696G= ENSP00000386741.3:p.Gln232=
ENST00000413882.5:c.150G= ENSP00000410496.1:p.Gln50=
ENST00000425395.5:c.*247G= ENSP00000405270.1:n.*247G=
ENST00000443238.5:c.174G= ENSP00000409798.1:p.Gln58=
ENST00000444394.5:c.21G= ENSP00000411911.1:p.Gln7=
ENST00000444573.1:c.321G= ENSP00000392603.1:p.Gln107=
ENST00000485882.1:n.155G=
ENST00000488080.5:n.547G=
NM_001025201.3:c.618G= NP_001020372.2:p.Gln206=
NM_001206602.1:c.321G= NP_001193531.1:p.Gln107=
NM_001822.5:c.696G= NP_001813.1:p.Gln232=
NR_038133.1:n.562G=
NM_001025201.4:c.618G= NP_001020372.2:p.Gln206=
NM_001206602.2:c.321G= NP_001193531.1:p.Gln107=
NM_001371513.1:c.696G= NP_001358442.1:p.Gln232=
NM_001371514.1:c.747G= NP_001358443.1:p.Gln249=
NM_001822.7:c.696G= MANE Select NP_001813.1:p.Gln232=
NR_038133.2:n.564G=