Canonical Allele Identifier: CA2754842675

Gene: HDAC4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.239191176_239191177insAGT , CM000664.2:g.239191176_239191177insAGT	GRCh38
NC_000002.11:g.240112872_240112873insAGT , CM000664.1:g.240112872_240112873insAGT	GRCh37
NC_000002.10:g.239777809_239777810insAGT	NCBI36
NG_009235.1:g.214771_214772insACT

Transcript Alleles

HGVS	Amino-acid change
ENST00000685474.1:n.581-1100_581-1099insACT
ENST00000543185.6:c.95-1100_95-1099insACT MANE Select	ENSP00000440481.3:n.95-1100_95-1099insACT
ENST00000345617.7:c.95-1100_95-1099insACT	ENSP00000264606.3:n.95-1100_95-1099insACT
ENST00000446876.1:c.14-1100_14-1099insACT	ENSP00000392912.1:n.14-1100_14-1099insACT
ENST00000463007.5:n.547-1100_547-1099insACT
ENST00000493582.5:n.567-1100_567-1099insACT
ENST00000496347.1:n.78-1100_78-1099insACT
ENST00000535493.5:n.438-1100_438-1099insACT
ENST00000543185.5:c.-257-1100_-257-1099insACT	ENSP00000440481.2:n.-257-1100_-257-1099insACT
NM_006037.3:c.95-1100_95-1099insACT	NP_006028.2:n.95-1100_95-1099insACT
XM_006712877.2:c.167-1100_167-1099insACT	XP_006712940.1:n.167-1100_167-1099insACT
XM_006712878.2:c.95-1100_95-1099insACT	XP_006712941.1:n.95-1100_95-1099insACT
XM_006712879.2:c.14-1100_14-1099insACT	XP_006712942.1:n.14-1100_14-1099insACT
XM_006712880.2:c.14-1100_14-1099insACT	XP_006712943.1:n.14-1100_14-1099insACT
XM_011512217.1:c.167-1100_167-1099insACT	XP_011510519.1:n.167-1100_167-1099insACT
XM_011512218.1:c.167-1100_167-1099insACT	XP_011510520.1:n.167-1100_167-1099insACT
XM_011512219.1:c.167-1100_167-1099insACT	XP_011510521.1:n.167-1100_167-1099insACT
XM_011512220.1:c.98-1100_98-1099insACT	XP_011510522.1:n.98-1100_98-1099insACT
XM_011512221.1:c.95-1100_95-1099insACT	XP_011510523.1:n.95-1100_95-1099insACT
XM_011512222.1:c.95-1100_95-1099insACT	XP_011510524.1:n.95-1100_95-1099insACT
XM_011512223.1:c.95-1100_95-1099insACT	XP_011510525.1:n.95-1100_95-1099insACT
XM_011512224.1:c.80-1100_80-1099insACT	XP_011510526.1:n.80-1100_80-1099insACT
XM_011512225.1:c.80-1100_80-1099insACT	XP_011510527.1:n.80-1100_80-1099insACT
XM_011512226.1:c.23-1100_23-1099insACT	XP_011510528.1:n.23-1100_23-1099insACT
XM_011512227.1:c.-50-1100_-50-1099insACT	XP_011510529.1:n.-50-1100_-50-1099insACT
XM_011512228.1:c.14-1100_14-1099insACT	XP_011510530.1:n.14-1100_14-1099insACT
XM_011512229.1:c.14-1100_14-1099insACT	XP_011510531.1:n.14-1100_14-1099insACT
XM_006712877.3:c.167-1100_167-1099insACT	XP_006712940.1:n.167-1100_167-1099insACT
XM_006712878.3:c.95-1100_95-1099insACT	XP_006712941.1:n.95-1100_95-1099insACT
XM_006712879.3:c.14-1100_14-1099insACT	XP_006712942.1:n.14-1100_14-1099insACT
XM_006712880.3:c.14-1100_14-1099insACT	XP_006712943.1:n.14-1100_14-1099insACT
XM_011512217.2:c.167-1100_167-1099insACT	XP_011510519.1:n.167-1100_167-1099insACT
XM_011512218.2:c.167-1100_167-1099insACT	XP_011510520.1:n.167-1100_167-1099insACT
XM_011512219.2:c.167-1100_167-1099insACT	XP_011510521.1:n.167-1100_167-1099insACT
XM_011512220.2:c.98-1100_98-1099insACT	XP_011510522.1:n.98-1100_98-1099insACT
XM_011512222.3:c.95-1100_95-1099insACT	XP_011510524.1:n.95-1100_95-1099insACT
XM_011512223.2:c.95-1100_95-1099insACT	XP_011510525.1:n.95-1100_95-1099insACT
XM_011512224.2:c.80-1100_80-1099insACT	XP_011510526.1:n.80-1100_80-1099insACT
XM_011512225.2:c.80-1100_80-1099insACT	XP_011510527.1:n.80-1100_80-1099insACT
XM_011512226.2:c.23-1100_23-1099insACT	XP_011510528.1:n.23-1100_23-1099insACT
XM_011512227.2:c.-50-1100_-50-1099insACT	XP_011510529.1:n.-50-1100_-50-1099insACT
XM_017005394.1:c.167-1100_167-1099insACT	XP_016860883.1:n.167-1100_167-1099insACT
XM_024453257.1:c.14-1100_14-1099insACT	XP_024309025.1:n.14-1100_14-1099insACT
NM_001378414.1:c.95-1100_95-1099insACT MANE Select	NP_001365343.1:n.95-1100_95-1099insACT
NM_001378415.1:c.95-1100_95-1099insACT	NP_001365344.1:n.95-1100_95-1099insACT
NM_001378416.1:c.95-1100_95-1099insACT	NP_001365345.1:n.95-1100_95-1099insACT
NM_001378417.1:c.95-1100_95-1099insACT	NP_001365346.1:n.95-1100_95-1099insACT
NM_006037.4:c.95-1100_95-1099insACT	NP_006028.2:n.95-1100_95-1099insACT