Canonical Allele Identifier: CA1308865824
Gene: CHN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.174824717C= , CM000664.2:g.174824717C= GRCh38
NC_000002.11:g.175689445C= , CM000664.1:g.175689445C= GRCh37
NC_000002.10:g.175397691C= NCBI36
NG_012642.1:g.185726G=
NG_012642.2:g.185726G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295497.13:c.253-199G= ENSP00000295497.7:n.253-199G=
ENST00000444394.7:c.253-199G= ENSP00000411911.2:n.253-199G=
ENST00000295497.12:c.253-199G= ENSP00000295497.7:n.253-199G=
ENST00000409089.7:c.-48-199G= ENSP00000386322.3:n.-48-199G=
ENST00000409900.9:c.628-199G= MANE Select ENSP00000386741.4:n.628-199G=
ENST00000413882.6:c.82-199G= ENSP00000410496.2:n.82-199G=
ENST00000425395.6:c.*75-199G= ENSP00000405270.2:n.*75-199G=
ENST00000443238.6:c.106-199G= ENSP00000409798.2:n.106-199G=
ENST00000444394.6:c.253-199G= ENSP00000411911.2:n.253-199G=
ENST00000444573.2:c.472-199G= ENSP00000392603.2:n.472-199G=
ENST00000451799.2:c.472-199G= ENSP00000416316.2:n.472-199G=
ENST00000469597.2:c.*276-199G= ENSP00000498417.1:n.*276-199G=
ENST00000488080.6:n.271-199G=
ENST00000650731.1:c.-48-199G= ENSP00000499146.1:n.-48-199G=
ENST00000650734.1:c.*528-199G= ENSP00000498742.1:n.*528-199G=
ENST00000650770.1:c.*542-199G= ENSP00000499036.1:n.*542-199G=
ENST00000650938.1:c.152-199G=
ENST00000651063.1:n.679-199G=
ENST00000651246.1:c.220-199G= ENSP00000498484.1:n.220-199G=
ENST00000651315.1:c.220-199G= ENSP00000498692.1:n.220-199G=
ENST00000651373.1:c.142-199G= ENSP00000499174.1:n.142-199G=
ENST00000651501.1:c.*75-199G= ENSP00000498894.1:n.*75-199G=
ENST00000651580.1:c.*207-199G= ENSP00000498631.1:n.*207-199G=
ENST00000651599.1:c.*112-199G= ENSP00000498535.1:n.*112-199G=
ENST00000651717.1:c.253-12235G= ENSP00000499124.1:n.253-12235G=
ENST00000651803.1:c.*620-199G= ENSP00000499007.1:n.*620-199G=
ENST00000651971.1:c.*428-199G= ENSP00000499035.1:n.*428-199G=
ENST00000652036.1:c.253-199G= ENSP00000499139.1:n.253-199G=
ENST00000652154.1:n.526-199G=
ENST00000652208.1:c.472-199G= ENSP00000498475.1:n.472-199G=
ENST00000652434.1:c.589-199G= ENSP00000498549.1:n.589-199G=
ENST00000652437.1:n.771-199G=
ENST00000652674.1:c.*112-199G= ENSP00000498599.1:n.*112-199G=
ENST00000652734.1:n.525-199G=
ENST00000652756.1:c.472-199G= ENSP00000498281.1:n.472-199G=
ENST00000652768.1:n.520-199G=
ENST00000295497.11:c.253-199G= ENSP00000295497.7:n.253-199G=
ENST00000409089.6:c.-48-199G= ENSP00000386322.2:n.-48-199G=
ENST00000409156.7:c.550-199G= ENSP00000386470.3:n.550-199G=
ENST00000409597.5:c.76-199G= ENSP00000386469.1:n.76-199G=
ENST00000409900.7:c.628-199G= ENSP00000386741.3:n.628-199G=
ENST00000413882.5:c.82-199G= ENSP00000410496.1:n.82-199G=
ENST00000425395.5:c.*179-199G= ENSP00000405270.1:n.*179-199G=
ENST00000443238.5:c.106-199G= ENSP00000409798.1:n.106-199G=
ENST00000444394.5:c.-48-199G= ENSP00000411911.1:n.-48-199G=
ENST00000444573.1:c.253-199G= ENSP00000392603.1:n.253-199G=
ENST00000485882.1:n.87-199G=
ENST00000488080.5:n.479-199G=
NM_001025201.3:c.550-199G= NP_001020372.2:n.550-199G=
NM_001206602.1:c.253-199G= NP_001193531.1:n.253-199G=
NM_001822.5:c.628-199G= NP_001813.1:n.628-199G=
NR_038133.1:n.494-199G=
NM_001025201.4:c.550-199G= NP_001020372.2:n.550-199G=
NM_001206602.2:c.253-199G= NP_001193531.1:n.253-199G=
NM_001371513.1:c.628-199G= NP_001358442.1:n.628-199G=
NM_001371514.1:c.679-199G= NP_001358443.1:n.679-199G=
NM_001822.7:c.628-199G= MANE Select NP_001813.1:n.628-199G=
NR_038133.2:n.496-199G=