Canonical Allele Identifier: CA2834843972

Gene: HDAC9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.18100687T>C , CM000669.2:g.18100687T>C	GRCh38
NC_000007.13:g.18140310T>C , CM000669.1:g.18140310T>C	GRCh37
NC_000007.12:g.18106835T>C	NCBI36
NG_023250.2:g.18739T>C
NG_023250.3:g.18739T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707077.1:c.-97+13474T>C	ENSP00000516728.1:n.-97+13474T>C
ENST00000417496.6:c.-97+13474T>C	ENSP00000401669.2:n.-97+13474T>C
ENST00000455069.1:n.153+12652T>C
NM_001204144.1:c.-97+13474T>C	NP_001191073.1:n.-97+13474T>C
XM_011515626.1:c.-97+12652T>C	XP_011513928.1:n.-97+12652T>C
XM_011515631.1:c.-97+13474T>C	XP_011513933.1:n.-97+13474T>C
NM_001204144.2:c.-97+13474T>C	NP_001191073.1:n.-97+13474T>C
NM_001321868.1:c.-97+13474T>C	NP_001308797.1:n.-97+13474T>C
NM_001321869.1:c.-97+13474T>C	NP_001308798.1:n.-97+13474T>C
NM_001321870.1:c.-97+13474T>C	NP_001308799.1:n.-97+13474T>C
NM_001321871.1:c.-97+13474T>C	NP_001308800.1:n.-97+13474T>C
NM_001321872.1:c.-97+13474T>C	NP_001308801.1:n.-97+13474T>C
NM_001321873.1:c.-97+13474T>C	NP_001308802.1:n.-97+13474T>C
NM_001204144.3:c.-97+13474T>C	NP_001191073.1:n.-97+13474T>C
NM_001321868.2:c.-97+13474T>C	NP_001308797.1:n.-97+13474T>C
NM_001321869.2:c.-97+13474T>C	NP_001308798.1:n.-97+13474T>C
NM_001321870.2:c.-97+13474T>C	NP_001308799.1:n.-97+13474T>C
NM_001321871.2:c.-97+13474T>C	NP_001308800.1:n.-97+13474T>C
NM_001321872.2:c.-97+13474T>C	NP_001308801.1:n.-97+13474T>C
NM_001321873.2:c.-97+13474T>C	NP_001308802.1:n.-97+13474T>C