Canonical Allele Identifier: CA2120748963
Gene: CHAMP1 HGNC NCBI

Linked Data

dbSNP Id: rs2087227299

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.114325085_114325086insC , CM000675.2:g.114325085_114325086insC GRCh38
NC_000013.10:g.115090560_115090561insC , CM000675.1:g.115090560_115090561insC GRCh37
NC_000013.9:g.114108662_114108663insC NCBI36
NG_051829.1:g.15751_15752insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000643483.2:c.1243_1244insC ENSP00000496699.1:p.Val415AlafsTer18
ENST00000644294.2:c.1243_1244insC ENSP00000495985.2:p.Val415AlafsTer18
ENST00000645174.2:c.1243_1244insC ENSP00000494031.2:p.Val415AlafsTer18
ENST00000700527.1:c.1243_1244insC ENSP00000515032.1:p.Val415AlafsTer18
ENST00000700528.1:c.1243_1244insC ENSP00000515033.1:p.Val415AlafsTer18
ENST00000361283.4:c.1243_1244insC MANE Select ENSP00000354730.1:p.Val415AlafsTer18
ENST00000643483.1:c.1243_1244insC ENSP00000496699.1:p.Val415AlafsTer18
ENST00000646155.1:n.123+10442_123+10443insC
ENST00000646956.1:n.285+3853_285+3854insC
ENST00000361283.2:c.1243_1244insC ENSP00000354730.1:p.Val415AlafsTer18
NM_001164144.1:c.1243_1244insC NP_001157616.1:p.Val415AlafsTer18
NM_001164145.1:c.1243_1244insC NP_001157617.1:p.Val415AlafsTer18
NM_032436.2:c.1243_1244insC NP_115812.1:p.Val415AlafsTer18
NM_001164144.2:c.1243_1244insC NP_001157616.1:p.Val415AlafsTer18
NM_001164145.2:c.1243_1244insC NP_001157617.1:p.Val415AlafsTer18
NM_032436.3:c.1243_1244insC NP_115812.1:p.Val415AlafsTer18
NM_032436.4:c.1243_1244insC MANE Select NP_115812.1:p.Val415AlafsTer18
NM_001164144.3:c.1243_1244insC NP_001157616.1:p.Val415AlafsTer18
NM_001164145.3:c.1243_1244insC NP_001157617.1:p.Val415AlafsTer18