Canonical Allele Identifier: CA1434092682

Gene: HTT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.3177388G= , CM000666.2:g.3177388G=	GRCh38
NC_000004.11:g.3179115G= , CM000666.1:g.3179115G=	GRCh37
NC_000004.10:g.3148913G=	NCBI36
NG_009378.1:g.107714G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355072.11:c.4463+1G= MANE Select	ENSP00000347184.5:n.4463+1G=
ENST00000355072.10:c.4463+1G=	ENSP00000347184.5:n.4463+1G=
ENST00000680239.1:c.4205+1G=	ENSP00000506169.1:n.4205+1G=
ENST00000680291.1:n.4560+1G=
ENST00000680360.1:c.4205+1G=	ENSP00000505014.1:n.4205+1G=
ENST00000680956.1:c.4205+1G=	ENSP00000506029.1:n.4205+1G=
ENST00000681528.1:c.4205+1G=	ENSP00000506116.1:n.4205+1G=
ENST00000355072.9:c.4463+1G=	ENSP00000347184.5:n.4463+1G=
ENST00000510626.5:n.4562+1G=
NM_002111.7:c.4469+1G=	NP_002102.4:n.4469+1G=
NM_002111.8:c.4469+1G=	NP_002102.4:n.4469+1G=
NM_001388492.1:c.4463+1G= MANE Select	NP_001375421.1:n.4463+1G=