Canonical Allele Identifier: CA154927281

Gene: HDAC9

Linked Data

• dbSNP Id: rs771848839
• MyVariant Identifiers: chr7:g.18140474A>G (hg19) ; chr7:g.18100851A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.18100851A>G , CM000669.2:g.18100851A>G	GRCh38
NC_000007.13:g.18140474A>G , CM000669.1:g.18140474A>G	GRCh37
NC_000007.12:g.18106999A>G	NCBI36
NG_023250.2:g.18903A>G
NG_023250.3:g.18903A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707077.1:c.-97+13638A>G	ENSP00000516728.1:n.-97+13638A>G
ENST00000417496.6:c.-97+13638A>G	ENSP00000401669.2:n.-97+13638A>G
ENST00000455069.1:n.153+12816A>G
NM_001204144.1:c.-97+13638A>G	NP_001191073.1:n.-97+13638A>G
XM_011515626.1:c.-97+12816A>G	XP_011513928.1:n.-97+12816A>G
XM_011515631.1:c.-97+13638A>G	XP_011513933.1:n.-97+13638A>G
NM_001204144.2:c.-97+13638A>G	NP_001191073.1:n.-97+13638A>G
NM_001321868.1:c.-97+13638A>G	NP_001308797.1:n.-97+13638A>G
NM_001321869.1:c.-97+13638A>G	NP_001308798.1:n.-97+13638A>G
NM_001321870.1:c.-97+13638A>G	NP_001308799.1:n.-97+13638A>G
NM_001321871.1:c.-97+13638A>G	NP_001308800.1:n.-97+13638A>G
NM_001321872.1:c.-97+13638A>G	NP_001308801.1:n.-97+13638A>G
NM_001321873.1:c.-97+13638A>G	NP_001308802.1:n.-97+13638A>G
NM_001204144.3:c.-97+13638A>G	NP_001191073.1:n.-97+13638A>G
NM_001321868.2:c.-97+13638A>G	NP_001308797.1:n.-97+13638A>G
NM_001321869.2:c.-97+13638A>G	NP_001308798.1:n.-97+13638A>G
NM_001321870.2:c.-97+13638A>G	NP_001308799.1:n.-97+13638A>G
NM_001321871.2:c.-97+13638A>G	NP_001308800.1:n.-97+13638A>G
NM_001321872.2:c.-97+13638A>G	NP_001308801.1:n.-97+13638A>G
NM_001321873.2:c.-97+13638A>G	NP_001308802.1:n.-97+13638A>G