Canonical Allele Identifier: CA2120748873

Gene: CHAMP1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.114324891C= , CM000675.2:g.114324891C=	GRCh38
NC_000013.10:g.115090366C= , CM000675.1:g.115090366C=	GRCh37
NC_000013.9:g.114108468C=	NCBI36
NG_051829.1:g.15557C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000643483.2:c.1049C=	ENSP00000496699.1:p.Pro350=
ENST00000644294.2:c.1049C=	ENSP00000495985.2:p.Pro350=
ENST00000645174.2:c.1049C=	ENSP00000494031.2:p.Pro350=
ENST00000700527.1:c.1049C=	ENSP00000515032.1:p.Pro350=
ENST00000700528.1:c.1049C=	ENSP00000515033.1:p.Pro350=
ENST00000361283.4:c.1049C= MANE Select	ENSP00000354730.1:p.Pro350=
ENST00000643483.1:c.1049C=	ENSP00000496699.1:p.Pro350=
ENST00000646155.1:n.123+10248C=
ENST00000646956.1:n.285+3659C=
ENST00000361283.2:c.1049C=	ENSP00000354730.1:p.Pro350=
NM_001164144.1:c.1049C=	NP_001157616.1:p.Pro350=
NM_001164145.1:c.1049C=	NP_001157617.1:p.Pro350=
NM_032436.2:c.1049C=	NP_115812.1:p.Pro350=
NM_001164144.2:c.1049C=	NP_001157616.1:p.Pro350=
NM_001164145.2:c.1049C=	NP_001157617.1:p.Pro350=
NM_032436.3:c.1049C=	NP_115812.1:p.Pro350=
NM_032436.4:c.1049C= MANE Select	NP_115812.1:p.Pro350=
NM_001164144.3:c.1049C=	NP_001157616.1:p.Pro350=
NM_001164145.3:c.1049C=	NP_001157617.1:p.Pro350=