Canonical Allele Identifier: CA2830555187

Gene: CHAMP1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.114325034_114325035insAT , CM000675.2:g.114325034_114325035insAT	GRCh38
NC_000013.10:g.115090509_115090510insAT , CM000675.1:g.115090509_115090510insAT	GRCh37
NC_000013.9:g.114108611_114108612insAT	NCBI36
NG_051829.1:g.15700_15701insAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643483.2:c.1192_1193insAT	ENSP00000496699.1:p.Arg398HisfsTer?
ENST00000644294.2:c.1192_1193insAT	ENSP00000495985.2:p.Arg398HisfsTer?
ENST00000645174.2:c.1192_1193insAT	ENSP00000494031.2:p.Arg398HisfsTer?
ENST00000700527.1:c.1192_1193insAT	ENSP00000515032.1:p.Arg398HisfsTer?
ENST00000700528.1:c.1192_1193insAT	ENSP00000515033.1:p.Arg398HisfsTer?
ENST00000361283.4:c.1192_1193insAT MANE Select	ENSP00000354730.1:p.Arg398HisfsTer?
ENST00000643483.1:c.1192_1193insAT	ENSP00000496699.1:p.Arg398HisfsTer?
ENST00000646155.1:n.123+10391_123+10392insAT
ENST00000646956.1:n.285+3802_285+3803insAT
ENST00000361283.2:c.1192_1193insAT	ENSP00000354730.1:p.Arg398HisfsTer?
NM_001164144.1:c.1192_1193insAT	NP_001157616.1:p.Arg398HisfsTer?
NM_001164145.1:c.1192_1193insAT	NP_001157617.1:p.Arg398HisfsTer?
NM_032436.2:c.1192_1193insAT	NP_115812.1:p.Arg398HisfsTer?
NM_001164144.2:c.1192_1193insAT	NP_001157616.1:p.Arg398HisfsTer?
NM_001164145.2:c.1192_1193insAT	NP_001157617.1:p.Arg398HisfsTer?
NM_032436.3:c.1192_1193insAT	NP_115812.1:p.Arg398HisfsTer?
NM_032436.4:c.1192_1193insAT MANE Select	NP_115812.1:p.Arg398HisfsTer?
NM_001164144.3:c.1192_1193insAT	NP_001157616.1:p.Arg398HisfsTer?
NM_001164145.3:c.1192_1193insAT	NP_001157617.1:p.Arg398HisfsTer?