Canonical Allele Identifier: CA2120748865
Gene: CHAMP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.114324871_114324904delinsGTCTCCTGGACCTTGGAAACCAATTCCTTCTGTA , CM000675.2:g.114324871_114324904delinsGTCTCCTGGACCTTGGAAACCAATTCCTTCTGTA GRCh38
NC_000013.10:g.115090346_115090379delinsGTCTCCTGGACCTTGGAAACCAATTCCTTCTGTA , CM000675.1:g.115090346_115090379delinsGTCTCCTGGACCTTGGAAACCAATTCCTTCTGTA GRCh37
NC_000013.9:g.114108448_114108481delinsGTCTCCTGGACCTTGGAAACCAATTCCTTCTGTA NCBI36
NG_051829.1:g.15537_15570delinsGTCTCCTGGACCTTGGAAACCAATTCCTTCTGTA

Transcript Alleles

HGVS Amino-acid change
ENST00000643483.2:c.1029_1062delinsGTCTCCTGGACCTTGGAAACCAATTCCTTCTGTA ENSP00000496699.1:p.Val343=
ENST00000644294.2:c.1029_1062delinsGTCTCCTGGACCTTGGAAACCAATTCCTTCTGTA ENSP00000495985.2:p.Val343=
ENST00000645174.2:c.1029_1062delinsGTCTCCTGGACCTTGGAAACCAATTCCTTCTGTA ENSP00000494031.2:p.Val343=
ENST00000700527.1:c.1029_1062delinsGTCTCCTGGACCTTGGAAACCAATTCCTTCTGTA ENSP00000515032.1:p.Val343=
ENST00000700528.1:c.1029_1062delinsGTCTCCTGGACCTTGGAAACCAATTCCTTCTGTA ENSP00000515033.1:p.Val343=
ENST00000361283.4:c.1029_1062delinsGTCTCCTGGACCTTGGAAACCAATTCCTTCTGTA MANE Select ENSP00000354730.1:p.Val343=
ENST00000643483.1:c.1029_1062delinsGTCTCCTGGACCTTGGAAACCAATTCCTTCTGTA ENSP00000496699.1:p.Val343=
ENST00000646155.1:n.123+10228_123+10261delinsGTCTCCTGGACCTTGGAAACCAATTCCTTCTGTA
ENST00000646956.1:n.285+3639_285+3672delinsGTCTCCTGGACCTTGGAAACCAATTCCTTCTGTA
ENST00000361283.2:c.1029_1062delinsGTCTCCTGGACCTTGGAAACCAATTCCTTCTGTA ENSP00000354730.1:p.Val343=
NM_001164144.1:c.1029_1062delinsGTCTCCTGGACCTTGGAAACCAATTCCTTCTGTA NP_001157616.1:p.Val343=
NM_001164145.1:c.1029_1062delinsGTCTCCTGGACCTTGGAAACCAATTCCTTCTGTA NP_001157617.1:p.Val343=
NM_032436.2:c.1029_1062delinsGTCTCCTGGACCTTGGAAACCAATTCCTTCTGTA NP_115812.1:p.Val343=
NM_001164144.2:c.1029_1062delinsGTCTCCTGGACCTTGGAAACCAATTCCTTCTGTA NP_001157616.1:p.Val343=
NM_001164145.2:c.1029_1062delinsGTCTCCTGGACCTTGGAAACCAATTCCTTCTGTA NP_001157617.1:p.Val343=
NM_032436.3:c.1029_1062delinsGTCTCCTGGACCTTGGAAACCAATTCCTTCTGTA NP_115812.1:p.Val343=
NM_032436.4:c.1029_1062delinsGTCTCCTGGACCTTGGAAACCAATTCCTTCTGTA MANE Select NP_115812.1:p.Val343=
NM_001164144.3:c.1029_1062delinsGTCTCCTGGACCTTGGAAACCAATTCCTTCTGTA NP_001157616.1:p.Val343=
NM_001164145.3:c.1029_1062delinsGTCTCCTGGACCTTGGAAACCAATTCCTTCTGTA NP_001157617.1:p.Val343=