Canonical Allele Identifier: CA155131119

Gene: HDAC9

Linked Data

• dbSNP Id: rs1051083489
• gnomAD v2: 7-18375091-G-T
• gnomAD v3: 7-18335468-G-T
• gnomAD v4: 7-18335468-G-T
• MyVariant Identifiers: chr7:g.18375091G>T (hg19) ; chr7:g.18335468G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.18335468G>T , CM000669.2:g.18335468G>T	GRCh38
NC_000007.13:g.18375091G>T , CM000669.1:g.18375091G>T	GRCh37
NC_000007.12:g.18341616G>T	NCBI36
NG_023250.2:g.253520G>T
NG_023250.3:g.253520G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707077.1:c.26-160794G>T	ENSP00000516728.1:n.26-160794G>T
ENST00000413509.6:c.-42+44953G>T	ENSP00000412497.2:n.-42+44953G>T
ENST00000417496.6:c.26-123374G>T	ENSP00000401669.2:n.26-123374G>T
ENST00000433709.6:c.-111+44953G>T	ENSP00000409003.2:n.-111+44953G>T
ENST00000461159.6:n.94+44953G>T
ENST00000474742.1:n.66+44953G>T
NM_001204144.1:c.26-123374G>T	NP_001191073.1:n.26-123374G>T
XM_011515626.1:c.100+44953G>T	XP_011513928.1:n.100+44953G>T
XM_011515627.1:c.16+44953G>T	XP_011513929.1:n.16+44953G>T
XM_011515628.1:c.16+44953G>T	XP_011513930.1:n.16+44953G>T
XM_011515629.1:c.16+44953G>T	XP_011513931.1:n.16+44953G>T
XM_011515630.1:c.16+44953G>T	XP_011513932.1:n.16+44953G>T
XM_011515631.1:c.26-160794G>T	XP_011513933.1:n.26-160794G>T
XM_011515632.1:c.16+44953G>T	XP_011513934.1:n.16+44953G>T
XM_011515633.1:c.16+44953G>T	XP_011513935.1:n.16+44953G>T
XM_011515634.1:c.16+44953G>T	XP_011513936.1:n.16+44953G>T
XM_011515647.1:c.16+44953G>T	XP_011513949.1:n.16+44953G>T
XM_011515650.1:c.16+44953G>T	XP_011513952.1:n.16+44953G>T
XM_011515651.1:c.16+44953G>T	XP_011513953.1:n.16+44953G>T
XR_926952.1:n.75+44953G>T
NM_001204144.2:c.26-123374G>T	NP_001191073.1:n.26-123374G>T
NM_001321868.1:c.26-160794G>T	NP_001308797.1:n.26-160794G>T
NM_001321869.1:c.26-160794G>T	NP_001308798.1:n.26-160794G>T
NM_001321870.1:c.26-160794G>T	NP_001308799.1:n.26-160794G>T
NM_001321871.1:c.26-160794G>T	NP_001308800.1:n.26-160794G>T
NM_001321872.1:c.26-160794G>T	NP_001308801.1:n.26-160794G>T
NM_001321873.1:c.26-160794G>T	NP_001308802.1:n.26-160794G>T
NM_001321896.1:c.-194+44953G>T	NP_001308825.1:n.-194+44953G>T
NM_001204144.3:c.26-123374G>T	NP_001191073.1:n.26-123374G>T
NM_001321868.2:c.26-160794G>T	NP_001308797.1:n.26-160794G>T
NM_001321869.2:c.26-160794G>T	NP_001308798.1:n.26-160794G>T
NM_001321870.2:c.26-160794G>T	NP_001308799.1:n.26-160794G>T
NM_001321871.2:c.26-160794G>T	NP_001308800.1:n.26-160794G>T
NM_001321872.2:c.26-160794G>T	NP_001308801.1:n.26-160794G>T
NM_001321873.2:c.26-160794G>T	NP_001308802.1:n.26-160794G>T
NM_001321896.2:c.-194+44953G>T	NP_001308825.1:n.-194+44953G>T