Canonical Allele Identifier: CA2753246115

Gene: CHN1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.174824518_174824519insAGT , CM000664.2:g.174824518_174824519insAGT	GRCh38
NC_000002.11:g.175689246_175689247insAGT , CM000664.1:g.175689246_175689247insAGT	GRCh37
NC_000002.10:g.175397492_175397493insAGT	NCBI36
NG_012642.1:g.185924_185925insACT
NG_012642.2:g.185924_185925insACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295497.13:c.253-1_253insACT	ENSP00000295497.7:n.253-1_253insACT
ENST00000444394.7:c.253-1_253insACT	ENSP00000411911.2:n.253-1_253insACT
ENST00000295497.12:c.253-1_253insACT	ENSP00000295497.7:n.253-1_253insACT
ENST00000409089.7:c.-48-1_-48insACT	ENSP00000386322.3:n.-48-1_-48insACT
ENST00000409900.9:c.628-1_628insACT MANE Select	ENSP00000386741.4:n.628-1_628insACT
ENST00000413882.6:c.82-1_82insACT	ENSP00000410496.2:n.82-1_82insACT
ENST00000425395.6:c.*75-1_*75insACT	ENSP00000405270.2:n.*75-1_*75insACT
ENST00000443238.6:c.106-1_106insACT	ENSP00000409798.2:n.106-1_106insACT
ENST00000444394.6:c.253-1_253insACT	ENSP00000411911.2:n.253-1_253insACT
ENST00000444573.2:c.472-1_472insACT	ENSP00000392603.2:n.472-1_472insACT
ENST00000451799.2:c.472-1_472insACT	ENSP00000416316.2:n.472-1_472insACT
ENST00000469597.2:c.*276-1_*276insACT	ENSP00000498417.1:n.*276-1_*276insACT
ENST00000488080.6:n.271-1_271insACT
ENST00000650731.1:c.-48-1_-48insACT	ENSP00000499146.1:n.-48-1_-48insACT
ENST00000650734.1:c.*528-1_*528insACT	ENSP00000498742.1:n.*528-1_*528insACT
ENST00000650770.1:c.*542-1_*542insACT	ENSP00000499036.1:n.*542-1_*542insACT
ENST00000650938.1:c.152-1_152insACT
ENST00000651063.1:n.679-1_679insACT
ENST00000651246.1:c.220-1_220insACT	ENSP00000498484.1:n.220-1_220insACT
ENST00000651315.1:c.220-1_220insACT	ENSP00000498692.1:n.220-1_220insACT
ENST00000651373.1:c.142-1_142insACT	ENSP00000499174.1:n.142-1_142insACT
ENST00000651501.1:c.*75-1_*75insACT	ENSP00000498894.1:n.*75-1_*75insACT
ENST00000651580.1:c.*207-1_*207insACT	ENSP00000498631.1:n.*207-1_*207insACT
ENST00000651599.1:c.*112-1_*112insACT	ENSP00000498535.1:n.*112-1_*112insACT
ENST00000651717.1:c.253-12037_253-12036insACT	ENSP00000499124.1:n.253-12037_253-12036insACT
ENST00000651803.1:c.*620-1_*620insACT	ENSP00000499007.1:n.*620-1_*620insACT
ENST00000651971.1:c.*428-1_*428insACT	ENSP00000499035.1:n.*428-1_*428insACT
ENST00000652036.1:c.253-1_253insACT	ENSP00000499139.1:n.253-1_253insACT
ENST00000652154.1:n.526-1_526insACT
ENST00000652208.1:c.472-1_472insACT	ENSP00000498475.1:n.472-1_472insACT
ENST00000652434.1:c.589-1_589insACT	ENSP00000498549.1:n.589-1_589insACT
ENST00000652437.1:n.771-1_771insACT
ENST00000652674.1:c.*112-1_*112insACT	ENSP00000498599.1:n.*112-1_*112insACT
ENST00000652734.1:n.525-1_525insACT
ENST00000652756.1:c.472-1_472insACT	ENSP00000498281.1:n.472-1_472insACT
ENST00000652768.1:n.520-1_520insACT
ENST00000295497.11:c.253-1_253insACT	ENSP00000295497.7:n.253-1_253insACT
ENST00000409089.6:c.-48-1_-48insACT	ENSP00000386322.2:n.-48-1_-48insACT
ENST00000409156.7:c.550-1_550insACT	ENSP00000386470.3:n.550-1_550insACT
ENST00000409597.5:c.76-1_76insACT	ENSP00000386469.1:n.76-1_76insACT
ENST00000409900.7:c.628-1_628insACT	ENSP00000386741.3:n.628-1_628insACT
ENST00000413882.5:c.82-1_82insACT	ENSP00000410496.1:n.82-1_82insACT
ENST00000425395.5:c.*179-1_*179insACT	ENSP00000405270.1:n.*179-1_*179insACT
ENST00000443238.5:c.106-1_106insACT	ENSP00000409798.1:n.106-1_106insACT
ENST00000444394.5:c.-48-1_-48insACT	ENSP00000411911.1:n.-48-1_-48insACT
ENST00000444573.1:c.253-1_253insACT	ENSP00000392603.1:n.253-1_253insACT
ENST00000485882.1:n.87-1_87insACT
ENST00000488080.5:n.479-1_479insACT
NM_001025201.3:c.550-1_550insACT	NP_001020372.2:n.550-1_550insACT
NM_001206602.1:c.253-1_253insACT	NP_001193531.1:n.253-1_253insACT
NM_001822.5:c.628-1_628insACT	NP_001813.1:n.628-1_628insACT
NR_038133.1:n.494-1_494insACT
NM_001025201.4:c.550-1_550insACT	NP_001020372.2:n.550-1_550insACT
NM_001206602.2:c.253-1_253insACT	NP_001193531.1:n.253-1_253insACT
NM_001371513.1:c.628-1_628insACT	NP_001358442.1:n.628-1_628insACT
NM_001371514.1:c.679-1_679insACT	NP_001358443.1:n.679-1_679insACT
NM_001822.7:c.628-1_628insACT MANE Select	NP_001813.1:n.628-1_628insACT
NR_038133.2:n.496-1_496insACT