Canonical Allele Identifier: CA1434037185
Gene: HTT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.3060499_3060500delinsAC , CM000666.2:g.3060499_3060500delinsAC GRCh38
NC_000004.11:g.3062226_3062227delinsAC , CM000666.1:g.3062226_3062227delinsAC GRCh37
NC_000004.10:g.3032024_3032025delinsAC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000647962.1:n.825-1977_825-1976delinsAC
ENST00000649900.1:n.503+18254_503+18255delinsAC
ENST00000680239.1:c.5+18254_5+18255delinsAC ENSP00000506169.1:n.5+18254_5+18255delinsAC
ENST00000680360.1:c.5+18254_5+18255delinsAC ENSP00000505014.1:n.5+18254_5+18255delinsAC
ENST00000680956.1:c.5+18254_5+18255delinsAC ENSP00000506029.1:n.5+18254_5+18255delinsAC
ENST00000681528.1:c.5+18254_5+18255delinsAC ENSP00000506116.1:n.5+18254_5+18255delinsAC