Canonical Allele Identifier: CA1692097632

Gene: HDAC9

Linked Data

• dbSNP Id: rs1796368703

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.18838302A>G , CM000669.2:g.18838302A>G	GRCh38
NC_000007.13:g.18877925A>G , CM000669.1:g.18877925A>G	GRCh37
NC_000007.12:g.18844450A>G	NCBI36
NG_023250.2:g.756354A>G
NG_023250.3:g.756354A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000686413.1:c.2684+2305A>G MANE Select	ENSP00000509161.1:n.2684+2305A>G
ENST00000441542.7:c.2684+2305A>G	ENSP00000408617.2:n.2684+2305A>G
ENST00000401921.5:c.2552+2305A>G	ENSP00000383912.1:n.2552+2305A>G
ENST00000406451.8:c.2675+2305A>G	ENSP00000384657.3:n.2675+2305A>G
ENST00000432645.6:c.2675+2305A>G	ENSP00000410337.2:n.2675+2305A>G
ENST00000441542.6:c.2684+2305A>G	ENSP00000408617.2:n.2684+2305A>G
ENST00000483142.5:n.89+2305A>G
ENST00000490851.5:n.656+2305A>G
NM_058176.2:c.2675+2305A>G	NP_478056.1:n.2675+2305A>G
NM_178423.1:c.2675+2305A>G	NP_848510.1:n.2675+2305A>G
NM_178425.2:c.2684+2305A>G	NP_848512.1:n.2684+2305A>G
XM_011515626.1:c.2840+2305A>G	XP_011513928.1:n.2840+2305A>G
XM_011515627.1:c.2750+2305A>G	XP_011513929.1:n.2750+2305A>G
XM_011515628.1:c.2747+2305A>G	XP_011513930.1:n.2747+2305A>G
XM_011515629.1:c.2741+2305A>G	XP_011513931.1:n.2741+2305A>G
XM_011515630.1:c.2735+2305A>G	XP_011513932.1:n.2735+2305A>G
XM_011515631.1:c.2765+2305A>G	XP_011513933.1:n.2765+2305A>G
XM_011515632.1:c.2756+2305A>G	XP_011513934.1:n.2756+2305A>G
XM_011515633.1:c.2624+2305A>G	XP_011513935.1:n.2624+2305A>G
XM_011515634.1:c.2609+2305A>G	XP_011513936.1:n.2609+2305A>G
XM_011515635.1:c.2699+2305A>G	XP_011513937.1:n.2699+2305A>G
XM_011515636.1:c.2690+2305A>G	XP_011513938.1:n.2690+2305A>G
XM_011515637.1:c.2690+2305A>G	XP_011513939.1:n.2690+2305A>G
XM_011515638.1:c.2684+2305A>G	XP_011513940.1:n.2684+2305A>G
XM_011515639.1:c.2684+2305A>G	XP_011513941.1:n.2684+2305A>G
XM_011515640.1:c.2606+2305A>G	XP_011513942.1:n.2606+2305A>G
XM_011515641.1:c.2606+2305A>G	XP_011513943.1:n.2606+2305A>G
XM_011515642.1:c.2606+2305A>G	XP_011513944.1:n.2606+2305A>G
XM_011515643.1:c.2606+2305A>G	XP_011513945.1:n.2606+2305A>G
XM_011515644.1:c.2591+2305A>G	XP_011513946.1:n.2591+2305A>G
XM_011515645.1:c.2591+2305A>G	XP_011513947.1:n.2591+2305A>G
XM_011515646.1:c.2582+2305A>G	XP_011513948.1:n.2582+2305A>G
XM_011515647.1:c.2756+2305A>G	XP_011513949.1:n.2756+2305A>G
XM_011515648.1:c.2699+2305A>G	XP_011513950.1:n.2699+2305A>G
XM_011515649.1:c.2699+2305A>G	XP_011513951.1:n.2699+2305A>G
NM_001321868.1:c.2609+2305A>G	NP_001308797.1:n.2609+2305A>G
NM_001321877.1:c.2552+2305A>G	NP_001308806.1:n.2552+2305A>G
NM_001321897.1:c.2552+2305A>G	NP_001308826.1:n.2552+2305A>G
NM_178423.2:c.2675+2305A>G	NP_848510.1:n.2675+2305A>G
NM_178425.3:c.2684+2305A>G	NP_848512.1:n.2684+2305A>G
NM_001321868.2:c.2609+2305A>G	NP_001308797.1:n.2609+2305A>G
NM_001321877.2:c.2552+2305A>G	NP_001308806.1:n.2552+2305A>G
NM_001321897.2:c.2552+2305A>G	NP_001308826.1:n.2552+2305A>G
NM_178423.3:c.2675+2305A>G	NP_848510.1:n.2675+2305A>G
NM_178425.4:c.2684+2305A>G MANE Select	NP_848512.1:n.2684+2305A>G