Canonical Allele Identifier: CA1691730571

Gene: HDAC9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.18101066T= , CM000669.2:g.18101066T=	GRCh38
NC_000007.13:g.18140689T= , CM000669.1:g.18140689T=	GRCh37
NC_000007.12:g.18107214T=	NCBI36
NG_023250.2:g.19118T=
NG_023250.3:g.19118T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707077.1:c.-97+13853T=	ENSP00000516728.1:n.-97+13853T=
ENST00000417496.6:c.-97+13853T=	ENSP00000401669.2:n.-97+13853T=
ENST00000455069.1:n.153+13031T=
NM_001204144.1:c.-97+13853T=	NP_001191073.1:n.-97+13853T=
XM_011515626.1:c.-97+13031T=	XP_011513928.1:n.-97+13031T=
XM_011515631.1:c.-97+13853T=	XP_011513933.1:n.-97+13853T=
NM_001204144.2:c.-97+13853T=	NP_001191073.1:n.-97+13853T=
NM_001321868.1:c.-97+13853T=	NP_001308797.1:n.-97+13853T=
NM_001321869.1:c.-97+13853T=	NP_001308798.1:n.-97+13853T=
NM_001321870.1:c.-97+13853T=	NP_001308799.1:n.-97+13853T=
NM_001321871.1:c.-97+13853T=	NP_001308800.1:n.-97+13853T=
NM_001321872.1:c.-97+13853T=	NP_001308801.1:n.-97+13853T=
NM_001321873.1:c.-97+13853T=	NP_001308802.1:n.-97+13853T=
NM_001204144.3:c.-97+13853T=	NP_001191073.1:n.-97+13853T=
NM_001321868.2:c.-97+13853T=	NP_001308797.1:n.-97+13853T=
NM_001321869.2:c.-97+13853T=	NP_001308798.1:n.-97+13853T=
NM_001321870.2:c.-97+13853T=	NP_001308799.1:n.-97+13853T=
NM_001321871.2:c.-97+13853T=	NP_001308800.1:n.-97+13853T=
NM_001321872.2:c.-97+13853T=	NP_001308801.1:n.-97+13853T=
NM_001321873.2:c.-97+13853T=	NP_001308802.1:n.-97+13853T=