Canonical Allele Identifier: CA2800706810
Gene: CHAMP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.114324617_114324624del , CM000675.2:g.114324617_114324624del GRCh38
NC_000013.10:g.115090092_115090099del , CM000675.1:g.115090092_115090099del GRCh37
NC_000013.9:g.114108194_114108201del NCBI36
NG_051829.1:g.15283_15290del

Transcript Alleles

HGVS Amino-acid Change
ENST00000643483.2:c.775_782del ENSP00000496699.1:p.Pro259SerfsTer16
ENST00000644294.2:c.775_782del ENSP00000495985.2:p.Pro259SerfsTer16
ENST00000645174.2:c.775_782del ENSP00000494031.2:p.Pro259SerfsTer16
ENST00000700527.1:c.775_782del ENSP00000515032.1:p.Pro259SerfsTer16
ENST00000700528.1:c.775_782del ENSP00000515033.1:p.Pro259SerfsTer16
ENST00000361283.4:c.775_782del MANE Select ENSP00000354730.1:p.Pro259SerfsTer16
ENST00000643483.1:c.775_782del ENSP00000496699.1:p.Pro259SerfsTer16
ENST00000646155.1:n.123+9974_123+9981del
ENST00000646956.1:n.285+3385_285+3392del
ENST00000361283.2:c.775_782del ENSP00000354730.1:p.Pro259SerfsTer16
NM_001164144.1:c.775_782del NP_001157616.1:p.Pro259SerfsTer16
NM_001164145.1:c.775_782del NP_001157617.1:p.Pro259SerfsTer16
NM_032436.2:c.775_782del NP_115812.1:p.Pro259SerfsTer16
NM_001164144.2:c.775_782del NP_001157616.1:p.Pro259SerfsTer16
NM_001164145.2:c.775_782del NP_001157617.1:p.Pro259SerfsTer16
NM_032436.3:c.775_782del NP_115812.1:p.Pro259SerfsTer16
NM_032436.4:c.775_782del MANE Select NP_115812.1:p.Pro259SerfsTer16
NM_001164144.3:c.775_782del NP_001157616.1:p.Pro259SerfsTer16
NM_001164145.3:c.775_782del NP_001157617.1:p.Pro259SerfsTer16