Canonical Allele Identifier: CA12628468

Gene: HDAC9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.18683609T>C , CM000669.2:g.18683609T>C	GRCh38
NC_000007.13:g.18723232T>C , CM000669.1:g.18723232T>C	GRCh37
NC_000007.12:g.18689757T>C	NCBI36
NG_023250.2:g.601661T>C
NG_023250.3:g.601661T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_178425.4:c.1731+17133T>C MANE Select	NP_848512.1:n.1731+17133T>C
ENST00000686413.1:c.1731+17133T>C MANE Select	ENSP00000509161.1:n.1731+17133T>C
NM_001321868.1:c.1656+17133T>C	NP_001308797.1:n.1656+17133T>C
NM_001321868.2:c.1656+17133T>C	NP_001308797.1:n.1656+17133T>C
NM_001321877.1:c.1599+17133T>C	NP_001308806.1:n.1599+17133T>C
NM_001321877.2:c.1599+17133T>C	NP_001308806.1:n.1599+17133T>C
NM_001321897.1:c.1599+17133T>C	NP_001308826.1:n.1599+17133T>C
NM_001321897.2:c.1599+17133T>C	NP_001308826.1:n.1599+17133T>C
NM_058176.2:c.1722+17133T>C	NP_478056.1:n.1722+17133T>C
NM_178423.1:c.1722+17133T>C	NP_848510.1:n.1722+17133T>C
NM_178423.2:c.1722+17133T>C	NP_848510.1:n.1722+17133T>C
NM_178423.3:c.1722+17133T>C	NP_848510.1:n.1722+17133T>C
NM_178425.2:c.1731+17133T>C	NP_848512.1:n.1731+17133T>C
NM_178425.3:c.1731+17133T>C	NP_848512.1:n.1731+17133T>C
ENST00000401921.5:c.1599+17133T>C	ENSP00000383912.1:n.1599+17133T>C
ENST00000406451.8:c.1722+17133T>C	ENSP00000384657.3:n.1722+17133T>C
ENST00000432645.6:c.1722+17133T>C	ENSP00000410337.2:n.1722+17133T>C
ENST00000441542.6:c.1731+17133T>C	ENSP00000408617.2:n.1731+17133T>C
ENST00000441542.7:c.1731+17133T>C	ENSP00000408617.2:n.1731+17133T>C
ENST00000461159.6:n.1734+17133T>C
ENST00000523867.5:n.1722+17133T>C
XM_011515626.1:c.1887+17133T>C	XP_011513928.1:n.1887+17133T>C
XM_011515627.1:c.1797+17133T>C	XP_011513929.1:n.1797+17133T>C
XM_011515628.1:c.1794+17133T>C	XP_011513930.1:n.1794+17133T>C
XM_011515629.1:c.1788+17133T>C	XP_011513931.1:n.1788+17133T>C
XM_011515630.1:c.1782+17133T>C	XP_011513932.1:n.1782+17133T>C
XM_011515631.1:c.1812+17133T>C	XP_011513933.1:n.1812+17133T>C
XM_011515632.1:c.1803+17133T>C	XP_011513934.1:n.1803+17133T>C
XM_011515633.1:c.1671+17133T>C	XP_011513935.1:n.1671+17133T>C
XM_011515634.1:c.1656+17133T>C	XP_011513936.1:n.1656+17133T>C
XM_011515635.1:c.1746+17133T>C	XP_011513937.1:n.1746+17133T>C
XM_011515636.1:c.1737+17133T>C	XP_011513938.1:n.1737+17133T>C
XM_011515637.1:c.1737+17133T>C	XP_011513939.1:n.1737+17133T>C
XM_011515638.1:c.1731+17133T>C	XP_011513940.1:n.1731+17133T>C
XM_011515639.1:c.1731+17133T>C	XP_011513941.1:n.1731+17133T>C
XM_011515640.1:c.1653+17133T>C	XP_011513942.1:n.1653+17133T>C
XM_011515641.1:c.1653+17133T>C	XP_011513943.1:n.1653+17133T>C
XM_011515642.1:c.1653+17133T>C	XP_011513944.1:n.1653+17133T>C
XM_011515643.1:c.1653+17133T>C	XP_011513945.1:n.1653+17133T>C
XM_011515644.1:c.1638+17133T>C	XP_011513946.1:n.1638+17133T>C
XM_011515645.1:c.1638+17133T>C	XP_011513947.1:n.1638+17133T>C
XM_011515646.1:c.1629+17133T>C	XP_011513948.1:n.1629+17133T>C
XM_011515647.1:c.1803+17133T>C	XP_011513949.1:n.1803+17133T>C
XM_011515648.1:c.1746+17133T>C	XP_011513950.1:n.1746+17133T>C
XM_011515649.1:c.1746+17133T>C	XP_011513951.1:n.1746+17133T>C
XM_011515650.1:c.1803+17133T>C	XP_011513952.1:n.1803+17133T>C
XR_926952.1:n.1862+17133T>C