Canonical Allele Identifier: CA1434111196

Gene: HTT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.3217326C= , CM000666.2:g.3217326C=	GRCh38
NC_000004.11:g.3219053C= , CM000666.1:g.3219053C=	GRCh37
NC_000004.10:g.3188851C=	NCBI36
NG_009378.1:g.147652C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355072.11:c.7055-439C= MANE Select	ENSP00000347184.5:n.7055-439C=
ENST00000355072.10:c.7055-439C=	ENSP00000347184.5:n.7055-439C=
ENST00000680239.1:c.6797-439C=	ENSP00000506169.1:n.6797-439C=
ENST00000680360.1:c.*262-439C=	ENSP00000505014.1:n.*262-439C=
ENST00000680956.1:c.6797-439C=	ENSP00000506029.1:n.6797-439C=
ENST00000681528.1:c.6887-439C=	ENSP00000506116.1:n.6887-439C=
ENST00000355072.9:c.7055-439C=	ENSP00000347184.5:n.7055-439C=
ENST00000510626.5:n.8183-439C=
NM_002111.7:c.7061-439C=	NP_002102.4:n.7061-439C=
NM_002111.8:c.7061-439C=	NP_002102.4:n.7061-439C=
NM_001388492.1:c.7055-439C= MANE Select	NP_001375421.1:n.7055-439C=