Canonical Allele Identifier: CA2172180634

Gene: CHP1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.41271783A= , CM000677.2:g.41271783A=	GRCh38
NC_000015.9:g.41563981A= , CM000677.1:g.41563981A=	GRCh37
NC_000015.8:g.39351273A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334660.10:c.411+1165A= MANE Select	ENSP00000335632.5:n.411+1165A=
ENST00000334660.9:c.411+1165A=	ENSP00000335632.5:n.411+1165A=
ENST00000392151.6:c.350-6984A=	ENSP00000440490.1:n.350-6984A=
ENST00000558351.5:n.543+1165A=
ENST00000560397.5:c.411+1165A=	ENSP00000454007.1:n.411+1165A=
ENST00000560411.5:c.*176+1165A=	ENSP00000453375.1:n.*176+1165A=
ENST00000560633.1:n.399-397A=
ENST00000560784.5:c.*110+1165A=	ENSP00000452772.1:n.*110+1165A=
ENST00000560965.1:c.272-397A=
NM_007236.4:c.411+1165A=	NP_009167.1:n.411+1165A=
NM_007236.5:c.411+1165A= MANE Select	NP_009167.1:n.411+1165A=