Canonical Allele Identifier: CA2662026468

Gene: CHN1

Linked Data

• gnomAD v4: 2-174877911-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.174877917dup , CM000664.2:g.174877917dup	GRCh38
NC_000002.11:g.175742645dup , CM000664.1:g.175742645dup	GRCh37
NC_000002.10:g.175450891dup	NCBI36
NG_012642.1:g.132531dup
NG_012642.2:g.132531dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000409900.9:c.477dup MANE Select	ENSP00000386741.4:p.His160ThrfsTer10
ENST00000425395.6:c.105-30955dup	ENSP00000405270.2:n.105-30955dup
ENST00000444573.2:c.321dup	ENSP00000392603.2:p.His108ThrfsTer10
ENST00000451799.2:c.321dup	ENSP00000416316.2:p.His108ThrfsTer10
ENST00000469597.2:c.*125dup	ENSP00000498417.1:n.*125dup
ENST00000488080.6:n.115-2047dup
ENST00000650734.1:c.*377dup	ENSP00000498742.1:n.*377dup
ENST00000650770.1:c.*391dup	ENSP00000499036.1:n.*391dup
ENST00000651063.1:n.528dup
ENST00000651246.1:c.69dup	ENSP00000498484.1:p.His24ThrfsTer10
ENST00000651315.1:c.69dup	ENSP00000498692.1:p.His24ThrfsTer10
ENST00000651373.1:c.69dup	ENSP00000499174.1:p.His24ThrfsTer10
ENST00000651501.1:c.105-30955dup	ENSP00000498894.1:n.105-30955dup
ENST00000651580.1:c.321dup	ENSP00000498631.1:p.His108ThrfsTer10
ENST00000651599.1:c.321dup	ENSP00000498535.1:p.His108ThrfsTer10
ENST00000651803.1:c.*391dup	ENSP00000499007.1:n.*391dup
ENST00000651971.1:c.*277dup	ENSP00000499035.1:n.*277dup
ENST00000652154.1:n.453dup
ENST00000652208.1:c.321dup	ENSP00000498475.1:p.His108ThrfsTer10
ENST00000652434.1:c.438dup	ENSP00000498549.1:p.His147ThrfsTer10
ENST00000652437.1:n.620dup
ENST00000652674.1:c.69dup	ENSP00000498599.1:p.His24ThrfsTer10
ENST00000652734.1:n.374dup
ENST00000652756.1:c.321dup	ENSP00000498281.1:p.His108ThrfsTer10
ENST00000652768.1:n.369dup
ENST00000409156.7:c.477dup	ENSP00000386470.3:p.His160ThrfsTer10
ENST00000409900.7:c.477dup	ENSP00000386741.3:p.His160ThrfsTer10
ENST00000425395.5:c.*101-30955dup	ENSP00000405270.1:n.*101-30955dup
ENST00000469597.1:n.582dup
ENST00000481174.1:n.30dup
ENST00000488080.5:n.401-30955dup
ENST00000490654.1:n.452dup
NM_001025201.3:c.477dup	NP_001020372.2:p.His160ThrfsTer10
NM_001822.5:c.477dup	NP_001813.1:p.His160ThrfsTer10
NR_038133.1:n.416-30955dup
NM_001025201.4:c.477dup	NP_001020372.2:p.His160ThrfsTer10
NM_001371513.1:c.477dup	NP_001358442.1:p.His160ThrfsTer10
NM_001371514.1:c.528dup	NP_001358443.1:p.His177ThrfsTer10
NM_001822.7:c.477dup MANE Select	NP_001813.1:p.His160ThrfsTer10
NR_038133.2:n.418-30955dup