Canonical Allele Identifier: CA1308865814
Gene: CHN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.174824689C= , CM000664.2:g.174824689C= GRCh38
NC_000002.11:g.175689417C= , CM000664.1:g.175689417C= GRCh37
NC_000002.10:g.175397663C= NCBI36
NG_012642.1:g.185754G=
NG_012642.2:g.185754G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295497.13:c.253-171G= ENSP00000295497.7:n.253-171G=
ENST00000444394.7:c.253-171G= ENSP00000411911.2:n.253-171G=
ENST00000295497.12:c.253-171G= ENSP00000295497.7:n.253-171G=
ENST00000409089.7:c.-48-171G= ENSP00000386322.3:n.-48-171G=
ENST00000409900.9:c.628-171G= MANE Select ENSP00000386741.4:n.628-171G=
ENST00000413882.6:c.82-171G= ENSP00000410496.2:n.82-171G=
ENST00000425395.6:c.*75-171G= ENSP00000405270.2:n.*75-171G=
ENST00000443238.6:c.106-171G= ENSP00000409798.2:n.106-171G=
ENST00000444394.6:c.253-171G= ENSP00000411911.2:n.253-171G=
ENST00000444573.2:c.472-171G= ENSP00000392603.2:n.472-171G=
ENST00000451799.2:c.472-171G= ENSP00000416316.2:n.472-171G=
ENST00000469597.2:c.*276-171G= ENSP00000498417.1:n.*276-171G=
ENST00000488080.6:n.271-171G=
ENST00000650731.1:c.-48-171G= ENSP00000499146.1:n.-48-171G=
ENST00000650734.1:c.*528-171G= ENSP00000498742.1:n.*528-171G=
ENST00000650770.1:c.*542-171G= ENSP00000499036.1:n.*542-171G=
ENST00000650938.1:c.152-171G=
ENST00000651063.1:n.679-171G=
ENST00000651246.1:c.220-171G= ENSP00000498484.1:n.220-171G=
ENST00000651315.1:c.220-171G= ENSP00000498692.1:n.220-171G=
ENST00000651373.1:c.142-171G= ENSP00000499174.1:n.142-171G=
ENST00000651501.1:c.*75-171G= ENSP00000498894.1:n.*75-171G=
ENST00000651580.1:c.*207-171G= ENSP00000498631.1:n.*207-171G=
ENST00000651599.1:c.*112-171G= ENSP00000498535.1:n.*112-171G=
ENST00000651717.1:c.253-12207G= ENSP00000499124.1:n.253-12207G=
ENST00000651803.1:c.*620-171G= ENSP00000499007.1:n.*620-171G=
ENST00000651971.1:c.*428-171G= ENSP00000499035.1:n.*428-171G=
ENST00000652036.1:c.253-171G= ENSP00000499139.1:n.253-171G=
ENST00000652154.1:n.526-171G=
ENST00000652208.1:c.472-171G= ENSP00000498475.1:n.472-171G=
ENST00000652434.1:c.589-171G= ENSP00000498549.1:n.589-171G=
ENST00000652437.1:n.771-171G=
ENST00000652674.1:c.*112-171G= ENSP00000498599.1:n.*112-171G=
ENST00000652734.1:n.525-171G=
ENST00000652756.1:c.472-171G= ENSP00000498281.1:n.472-171G=
ENST00000652768.1:n.520-171G=
ENST00000295497.11:c.253-171G= ENSP00000295497.7:n.253-171G=
ENST00000409089.6:c.-48-171G= ENSP00000386322.2:n.-48-171G=
ENST00000409156.7:c.550-171G= ENSP00000386470.3:n.550-171G=
ENST00000409597.5:c.76-171G= ENSP00000386469.1:n.76-171G=
ENST00000409900.7:c.628-171G= ENSP00000386741.3:n.628-171G=
ENST00000413882.5:c.82-171G= ENSP00000410496.1:n.82-171G=
ENST00000425395.5:c.*179-171G= ENSP00000405270.1:n.*179-171G=
ENST00000443238.5:c.106-171G= ENSP00000409798.1:n.106-171G=
ENST00000444394.5:c.-48-171G= ENSP00000411911.1:n.-48-171G=
ENST00000444573.1:c.253-171G= ENSP00000392603.1:n.253-171G=
ENST00000485882.1:n.87-171G=
ENST00000488080.5:n.479-171G=
NM_001025201.3:c.550-171G= NP_001020372.2:n.550-171G=
NM_001206602.1:c.253-171G= NP_001193531.1:n.253-171G=
NM_001822.5:c.628-171G= NP_001813.1:n.628-171G=
NR_038133.1:n.494-171G=
NM_001025201.4:c.550-171G= NP_001020372.2:n.550-171G=
NM_001206602.2:c.253-171G= NP_001193531.1:n.253-171G=
NM_001371513.1:c.628-171G= NP_001358442.1:n.628-171G=
NM_001371514.1:c.679-171G= NP_001358443.1:n.679-171G=
NM_001822.7:c.628-171G= MANE Select NP_001813.1:n.628-171G=
NR_038133.2:n.496-171G=