Canonical Allele Identifier: CA349689787
Gene: CHN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.174878018A>T , CM000664.2:g.174878018A>T GRCh38
NC_000002.11:g.175742746A>T , CM000664.1:g.175742746A>T GRCh37
NC_000002.10:g.175450992A>T NCBI36
NG_012642.1:g.132425T>A
NG_012642.2:g.132425T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000409900.9:c.371T>A MANE Select ENSP00000386741.4:p.Leu124His
ENST00000425395.6:c.105-31061T>A ENSP00000405270.2:n.105-31061T>A
ENST00000444573.2:c.215T>A ENSP00000392603.2:p.Leu72His
ENST00000451799.2:c.215T>A ENSP00000416316.2:p.Leu72His
ENST00000469597.2:c.*19T>A ENSP00000498417.1:n.*19T>A
ENST00000488080.6:n.115-2153T>A
ENST00000650734.1:c.*271T>A ENSP00000498742.1:n.*271T>A
ENST00000650770.1:c.*285T>A ENSP00000499036.1:n.*285T>A
ENST00000651063.1:n.422T>A
ENST00000651246.1:c.-38T>A ENSP00000498484.1:n.-38T>A
ENST00000651315.1:c.-38T>A ENSP00000498692.1:n.-38T>A
ENST00000651373.1:c.-38T>A ENSP00000499174.1:n.-38T>A
ENST00000651501.1:c.105-31061T>A ENSP00000498894.1:n.105-31061T>A
ENST00000651580.1:c.215T>A ENSP00000498631.1:p.Leu72His
ENST00000651599.1:c.215T>A ENSP00000498535.1:p.Leu72His
ENST00000651803.1:c.*285T>A ENSP00000499007.1:n.*285T>A
ENST00000651971.1:c.*171T>A ENSP00000499035.1:n.*171T>A
ENST00000652154.1:n.347T>A
ENST00000652208.1:c.215T>A ENSP00000498475.1:p.Leu72His
ENST00000652434.1:c.332T>A ENSP00000498549.1:p.Leu111His
ENST00000652437.1:n.514T>A
ENST00000652674.1:c.-38T>A ENSP00000498599.1:n.-38T>A
ENST00000652734.1:n.268T>A
ENST00000652756.1:c.215T>A ENSP00000498281.1:p.Leu72His
ENST00000652768.1:n.263T>A
ENST00000409156.7:c.371T>A ENSP00000386470.3:p.Leu124His
ENST00000409900.7:c.371T>A ENSP00000386741.3:p.Leu124His
ENST00000425395.5:c.*101-31061T>A ENSP00000405270.1:n.*101-31061T>A
ENST00000469597.1:n.476T>A
ENST00000488080.5:n.401-31061T>A
ENST00000490654.1:n.346T>A
NM_001025201.3:c.371T>A NP_001020372.2:p.Leu124His
NM_001822.5:c.371T>A NP_001813.1:p.Leu124His
NR_038133.1:n.416-31061T>A
NM_001025201.4:c.371T>A NP_001020372.2:p.Leu124His
NM_001371513.1:c.371T>A NP_001358442.1:p.Leu124His
NM_001371514.1:c.422T>A NP_001358443.1:p.Leu141His
NM_001822.7:c.371T>A MANE Select NP_001813.1:p.Leu124His
NR_038133.2:n.418-31061T>A