Canonical Allele Identifier: CA2701085310
Gene: CHN1 HGNC NCBI

Linked Data

dbSNP Id: rs2105402134

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.174824630_174824631insCATA , CM000664.2:g.174824630_174824631insCATA GRCh38
NC_000002.11:g.175689358_175689359insCATA , CM000664.1:g.175689358_175689359insCATA GRCh37
NC_000002.10:g.175397604_175397605insCATA NCBI36
NG_012642.1:g.185815_185816insGTAT
NG_012642.2:g.185815_185816insGTAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000295497.13:c.253-110_253-109insGTAT ENSP00000295497.7:n.253-110_253-109insGTAT
ENST00000444394.7:c.253-110_253-109insGTAT ENSP00000411911.2:n.253-110_253-109insGTAT
ENST00000295497.12:c.253-110_253-109insGTAT ENSP00000295497.7:n.253-110_253-109insGTAT
ENST00000409089.7:c.-48-110_-48-109insGTAT ENSP00000386322.3:n.-48-110_-48-109insGTAT
ENST00000409900.9:c.628-110_628-109insGTAT MANE Select ENSP00000386741.4:n.628-110_628-109insGTAT
ENST00000413882.6:c.82-110_82-109insGTAT ENSP00000410496.2:n.82-110_82-109insGTAT
ENST00000425395.6:c.*75-110_*75-109insGTAT ENSP00000405270.2:n.*75-110_*75-109insGTAT
ENST00000443238.6:c.106-110_106-109insGTAT ENSP00000409798.2:n.106-110_106-109insGTAT
ENST00000444394.6:c.253-110_253-109insGTAT ENSP00000411911.2:n.253-110_253-109insGTAT
ENST00000444573.2:c.472-110_472-109insGTAT ENSP00000392603.2:n.472-110_472-109insGTAT
ENST00000451799.2:c.472-110_472-109insGTAT ENSP00000416316.2:n.472-110_472-109insGTAT
ENST00000469597.2:c.*276-110_*276-109insGTAT ENSP00000498417.1:n.*276-110_*276-109insGTAT
ENST00000488080.6:n.271-110_271-109insGTAT
ENST00000650731.1:c.-48-110_-48-109insGTAT ENSP00000499146.1:n.-48-110_-48-109insGTAT
ENST00000650734.1:c.*528-110_*528-109insGTAT ENSP00000498742.1:n.*528-110_*528-109insGTAT
ENST00000650770.1:c.*542-110_*542-109insGTAT ENSP00000499036.1:n.*542-110_*542-109insGTAT
ENST00000650938.1:c.152-110_152-109insGTAT
ENST00000651063.1:n.679-110_679-109insGTAT
ENST00000651246.1:c.220-110_220-109insGTAT ENSP00000498484.1:n.220-110_220-109insGTAT
ENST00000651315.1:c.220-110_220-109insGTAT ENSP00000498692.1:n.220-110_220-109insGTAT
ENST00000651373.1:c.142-110_142-109insGTAT ENSP00000499174.1:n.142-110_142-109insGTAT
ENST00000651501.1:c.*75-110_*75-109insGTAT ENSP00000498894.1:n.*75-110_*75-109insGTAT
ENST00000651580.1:c.*207-110_*207-109insGTAT ENSP00000498631.1:n.*207-110_*207-109insGTAT
ENST00000651599.1:c.*112-110_*112-109insGTAT ENSP00000498535.1:n.*112-110_*112-109insGTAT
ENST00000651717.1:c.253-12146_253-12145insGTAT ENSP00000499124.1:n.253-12146_253-12145insGTAT
ENST00000651803.1:c.*620-110_*620-109insGTAT ENSP00000499007.1:n.*620-110_*620-109insGTAT
ENST00000651971.1:c.*428-110_*428-109insGTAT ENSP00000499035.1:n.*428-110_*428-109insGTAT
ENST00000652036.1:c.253-110_253-109insGTAT ENSP00000499139.1:n.253-110_253-109insGTAT
ENST00000652154.1:n.526-110_526-109insGTAT
ENST00000652208.1:c.472-110_472-109insGTAT ENSP00000498475.1:n.472-110_472-109insGTAT
ENST00000652434.1:c.589-110_589-109insGTAT ENSP00000498549.1:n.589-110_589-109insGTAT
ENST00000652437.1:n.771-110_771-109insGTAT
ENST00000652674.1:c.*112-110_*112-109insGTAT ENSP00000498599.1:n.*112-110_*112-109insGTAT
ENST00000652734.1:n.525-110_525-109insGTAT
ENST00000652756.1:c.472-110_472-109insGTAT ENSP00000498281.1:n.472-110_472-109insGTAT
ENST00000652768.1:n.520-110_520-109insGTAT
ENST00000295497.11:c.253-110_253-109insGTAT ENSP00000295497.7:n.253-110_253-109insGTAT
ENST00000409089.6:c.-48-110_-48-109insGTAT ENSP00000386322.2:n.-48-110_-48-109insGTAT
ENST00000409156.7:c.550-110_550-109insGTAT ENSP00000386470.3:n.550-110_550-109insGTAT
ENST00000409597.5:c.76-110_76-109insGTAT ENSP00000386469.1:n.76-110_76-109insGTAT
ENST00000409900.7:c.628-110_628-109insGTAT ENSP00000386741.3:n.628-110_628-109insGTAT
ENST00000413882.5:c.82-110_82-109insGTAT ENSP00000410496.1:n.82-110_82-109insGTAT
ENST00000425395.5:c.*179-110_*179-109insGTAT ENSP00000405270.1:n.*179-110_*179-109insGTAT
ENST00000443238.5:c.106-110_106-109insGTAT ENSP00000409798.1:n.106-110_106-109insGTAT
ENST00000444394.5:c.-48-110_-48-109insGTAT ENSP00000411911.1:n.-48-110_-48-109insGTAT
ENST00000444573.1:c.253-110_253-109insGTAT ENSP00000392603.1:n.253-110_253-109insGTAT
ENST00000485882.1:n.87-110_87-109insGTAT
ENST00000488080.5:n.479-110_479-109insGTAT
NM_001025201.3:c.550-110_550-109insGTAT NP_001020372.2:n.550-110_550-109insGTAT
NM_001206602.1:c.253-110_253-109insGTAT NP_001193531.1:n.253-110_253-109insGTAT
NM_001822.5:c.628-110_628-109insGTAT NP_001813.1:n.628-110_628-109insGTAT
NR_038133.1:n.494-110_494-109insGTAT
NM_001025201.4:c.550-110_550-109insGTAT NP_001020372.2:n.550-110_550-109insGTAT
NM_001206602.2:c.253-110_253-109insGTAT NP_001193531.1:n.253-110_253-109insGTAT
NM_001371513.1:c.628-110_628-109insGTAT NP_001358442.1:n.628-110_628-109insGTAT
NM_001371514.1:c.679-110_679-109insGTAT NP_001358443.1:n.679-110_679-109insGTAT
NM_001822.7:c.628-110_628-109insGTAT MANE Select NP_001813.1:n.628-110_628-109insGTAT
NR_038133.2:n.496-110_496-109insGTAT