Canonical Allele Identifier: CA2838338320

Gene: HDAC4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.239176619A>G , CM000664.2:g.239176619A>G	GRCh38
NC_000002.11:g.240098315A>G , CM000664.1:g.240098315A>G	GRCh37
NC_000002.10:g.239763252A>G	NCBI36
NG_009235.1:g.229329T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000543185.6:c.340-56T>C MANE Select	ENSP00000440481.3:n.340-56T>C
ENST00000345617.7:c.340-56T>C	ENSP00000264606.3:n.340-56T>C
ENST00000446876.1:c.259-56T>C	ENSP00000392912.1:n.259-56T>C
ENST00000454542.5:c.247-56T>C	ENSP00000405226.1:n.247-56T>C
ENST00000463007.5:n.792-56T>C
ENST00000493582.5:n.812-56T>C
ENST00000535493.5:n.683-56T>C
ENST00000543185.5:c.-12-56T>C	ENSP00000440481.2:n.-12-56T>C
NM_006037.3:c.340-56T>C	NP_006028.2:n.340-56T>C
XM_006712877.2:c.412-56T>C	XP_006712940.1:n.412-56T>C
XM_006712878.2:c.340-56T>C	XP_006712941.1:n.340-56T>C
XM_006712879.2:c.259-56T>C	XP_006712942.1:n.259-56T>C
XM_006712880.2:c.259-56T>C	XP_006712943.1:n.259-56T>C
XM_011512217.1:c.412-56T>C	XP_011510519.1:n.412-56T>C
XM_011512218.1:c.412-56T>C	XP_011510520.1:n.412-56T>C
XM_011512219.1:c.412-56T>C	XP_011510521.1:n.412-56T>C
XM_011512220.1:c.343-56T>C	XP_011510522.1:n.343-56T>C
XM_011512221.1:c.340-56T>C	XP_011510523.1:n.340-56T>C
XM_011512222.1:c.340-56T>C	XP_011510524.1:n.340-56T>C
XM_011512223.1:c.340-56T>C	XP_011510525.1:n.340-56T>C
XM_011512224.1:c.325-56T>C	XP_011510526.1:n.325-56T>C
XM_011512225.1:c.325-56T>C	XP_011510527.1:n.325-56T>C
XM_011512226.1:c.268-56T>C	XP_011510528.1:n.268-56T>C
XM_011512227.1:c.196-56T>C	XP_011510529.1:n.196-56T>C
XM_011512228.1:c.259-56T>C	XP_011510530.1:n.259-56T>C
XM_011512229.1:c.259-56T>C	XP_011510531.1:n.259-56T>C
XM_006712877.3:c.412-56T>C	XP_006712940.1:n.412-56T>C
XM_006712878.3:c.340-56T>C	XP_006712941.1:n.340-56T>C
XM_006712879.3:c.259-56T>C	XP_006712942.1:n.259-56T>C
XM_006712880.3:c.259-56T>C	XP_006712943.1:n.259-56T>C
XM_011512217.2:c.412-56T>C	XP_011510519.1:n.412-56T>C
XM_011512218.2:c.412-56T>C	XP_011510520.1:n.412-56T>C
XM_011512219.2:c.412-56T>C	XP_011510521.1:n.412-56T>C
XM_011512220.2:c.343-56T>C	XP_011510522.1:n.343-56T>C
XM_011512222.3:c.340-56T>C	XP_011510524.1:n.340-56T>C
XM_011512223.2:c.340-56T>C	XP_011510525.1:n.340-56T>C
XM_011512224.2:c.325-56T>C	XP_011510526.1:n.325-56T>C
XM_011512225.2:c.325-56T>C	XP_011510527.1:n.325-56T>C
XM_011512226.2:c.268-56T>C	XP_011510528.1:n.268-56T>C
XM_011512227.2:c.196-56T>C	XP_011510529.1:n.196-56T>C
XM_017005394.1:c.412-56T>C	XP_016860883.1:n.412-56T>C
XM_024453257.1:c.259-56T>C	XP_024309025.1:n.259-56T>C
NM_001378414.1:c.340-56T>C MANE Select	NP_001365343.1:n.340-56T>C
NM_001378415.1:c.340-56T>C	NP_001365344.1:n.340-56T>C
NM_001378416.1:c.340-56T>C	NP_001365345.1:n.340-56T>C
NM_001378417.1:c.340-56T>C	NP_001365346.1:n.340-56T>C
NM_006037.4:c.340-56T>C	NP_006028.2:n.340-56T>C