Canonical Allele Identifier: CA2172180645

Gene: CHP1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.41271799C= , CM000677.2:g.41271799C=	GRCh38
NC_000015.9:g.41563997C= , CM000677.1:g.41563997C=	GRCh37
NC_000015.8:g.39351289C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000334660.10:c.411+1181C= MANE Select	ENSP00000335632.5:n.411+1181C=
ENST00000334660.9:c.411+1181C=	ENSP00000335632.5:n.411+1181C=
ENST00000392151.6:c.350-6968C=	ENSP00000440490.1:n.350-6968C=
ENST00000558351.5:n.543+1181C=
ENST00000560397.5:c.411+1181C=	ENSP00000454007.1:n.411+1181C=
ENST00000560411.5:c.*176+1181C=	ENSP00000453375.1:n.*176+1181C=
ENST00000560633.1:n.399-381C=
ENST00000560784.5:c.*110+1181C=	ENSP00000452772.1:n.*110+1181C=
ENST00000560965.1:c.272-381C=
NM_007236.4:c.411+1181C=	NP_009167.1:n.411+1181C=
NM_007236.5:c.411+1181C= MANE Select	NP_009167.1:n.411+1181C=