Canonical Allele Identifier: CA2172180635

Gene: CHP1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.41271784A= , CM000677.2:g.41271784A=	GRCh38
NC_000015.9:g.41563982A= , CM000677.1:g.41563982A=	GRCh37
NC_000015.8:g.39351274A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334660.10:c.411+1166A= MANE Select	ENSP00000335632.5:n.411+1166A=
ENST00000334660.9:c.411+1166A=	ENSP00000335632.5:n.411+1166A=
ENST00000392151.6:c.350-6983A=	ENSP00000440490.1:n.350-6983A=
ENST00000558351.5:n.543+1166A=
ENST00000560397.5:c.411+1166A=	ENSP00000454007.1:n.411+1166A=
ENST00000560411.5:c.*176+1166A=	ENSP00000453375.1:n.*176+1166A=
ENST00000560633.1:n.399-396A=
ENST00000560784.5:c.*110+1166A=	ENSP00000452772.1:n.*110+1166A=
ENST00000560965.1:c.272-396A=
NM_007236.4:c.411+1166A=	NP_009167.1:n.411+1166A=
NM_007236.5:c.411+1166A= MANE Select	NP_009167.1:n.411+1166A=