Canonical Allele Identifier: CA1434035158
Gene: HTT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.3056082A= , CM000666.2:g.3056082A= GRCh38
NC_000004.11:g.3057809A= , CM000666.1:g.3057809A= GRCh37
NC_000004.10:g.3027607A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000647962.1:n.825-6394A=
ENST00000649900.1:n.503+13837A=
ENST00000680239.1:c.5+13837A= ENSP00000506169.1:n.5+13837A=
ENST00000680360.1:c.5+13837A= ENSP00000505014.1:n.5+13837A=
ENST00000680956.1:c.5+13837A= ENSP00000506029.1:n.5+13837A=
ENST00000681528.1:c.5+13837A= ENSP00000506116.1:n.5+13837A=