Canonical Allele Identifier: CA1338435903
Gene: HDAC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.239082181C= , CM000664.2:g.239082181C= GRCh38
NC_000002.11:g.240003877C= , CM000664.1:g.240003877C= GRCh37
NC_000002.10:g.239668814C= NCBI36
NG_009235.1:g.323767G=

Transcript Alleles

HGVS Amino-acid change
ENST00000690129.1:n.587G=
ENST00000543185.6:c.2573G= MANE Select ENSP00000440481.3:p.Ser858=
ENST00000345617.7:c.2558G= ENSP00000264606.3:p.Ser853=
ENST00000487617.5:n.465G=
ENST00000543185.5:c.2222G= ENSP00000440481.2:p.Ser741=
NM_006037.3:c.2558G= NP_006028.2:p.Ser853=
XM_006712877.2:c.2630G= XP_006712940.1:p.Ser877=
XM_006712878.2:c.2573G= XP_006712941.1:p.Ser858=
XM_006712879.2:c.2492G= XP_006712942.1:p.Ser831=
XM_006712880.2:c.2492G= XP_006712943.1:p.Ser831=
XM_011512217.1:c.2645G= XP_011510519.1:p.Ser882=
XM_011512218.1:c.2630G= XP_011510520.1:p.Ser877=
XM_011512219.1:c.2615G= XP_011510521.1:p.Ser872=
XM_011512220.1:c.2576G= XP_011510522.1:p.Ser859=
XM_011512221.1:c.2573G= XP_011510523.1:p.Ser858=
XM_011512222.1:c.2573G= XP_011510524.1:p.Ser858=
XM_011512223.1:c.2573G= XP_011510525.1:p.Ser858=
XM_011512224.1:c.2558G= XP_011510526.1:p.Ser853=
XM_011512225.1:c.2543G= XP_011510527.1:p.Ser848=
XM_011512226.1:c.2501G= XP_011510528.1:p.Ser834=
XM_011512227.1:c.2429G= XP_011510529.1:p.Ser810=
XM_011512228.1:c.2492G= XP_011510530.1:p.Ser831=
XM_011512229.1:c.2492G= XP_011510531.1:p.Ser831=
XM_011512230.1:c.1325G= XP_011510532.1:p.Ser442=
XM_006712877.3:c.2630G= XP_006712940.1:p.Ser877=
XM_006712878.3:c.2573G= XP_006712941.1:p.Ser858=
XM_006712879.3:c.2492G= XP_006712942.1:p.Ser831=
XM_006712880.3:c.2492G= XP_006712943.1:p.Ser831=
XM_011512217.2:c.2645G= XP_011510519.1:p.Ser882=
XM_011512218.2:c.2630G= XP_011510520.1:p.Ser877=
XM_011512219.2:c.2615G= XP_011510521.1:p.Ser872=
XM_011512220.2:c.2576G= XP_011510522.1:p.Ser859=
XM_011512222.3:c.2573G= XP_011510524.1:p.Ser858=
XM_011512223.2:c.2573G= XP_011510525.1:p.Ser858=
XM_011512224.2:c.2558G= XP_011510526.1:p.Ser853=
XM_011512225.2:c.2543G= XP_011510527.1:p.Ser848=
XM_011512226.2:c.2501G= XP_011510528.1:p.Ser834=
XM_011512227.2:c.2429G= XP_011510529.1:p.Ser810=
XM_017005394.1:c.2513G= XP_016860883.1:p.Ser838=
XM_017005395.1:c.2057G= XP_016860884.1:p.Ser686=
XM_024453257.1:c.2492G= XP_024309025.1:p.Ser831=
NM_001378414.1:c.2573G= MANE Select NP_001365343.1:p.Ser858=
NM_001378415.1:c.2573G= NP_001365344.1:p.Ser858=
NM_001378416.1:c.2558G= NP_001365345.1:p.Ser853=
NM_001378417.1:c.2558G= NP_001365346.1:p.Ser853=
NM_006037.4:c.2558G= NP_006028.2:p.Ser853=