Canonical Allele Identifier: CA351261881
Gene: HDAC4 HGNC NCBI

Linked Data

dbSNP Id: rs1191340912

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.239084225T>A , CM000664.2:g.239084225T>A GRCh38
NC_000002.11:g.240005921T>A , CM000664.1:g.240005921T>A GRCh37
NC_000002.10:g.239670858T>A NCBI36
NG_009235.1:g.321723A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000690129.1:n.476A>T
ENST00000543185.6:c.2462A>T MANE Select ENSP00000440481.3:p.Asn821Ile
ENST00000345617.7:c.2447A>T ENSP00000264606.3:p.Asn816Ile
ENST00000487617.5:n.354A>T
ENST00000543185.5:c.2111A>T ENSP00000440481.2:p.Asn704Ile
NM_006037.3:c.2447A>T NP_006028.2:p.Asn816Ile
XM_006712877.2:c.2519A>T XP_006712940.1:p.Asn840Ile
XM_006712878.2:c.2462A>T XP_006712941.1:p.Asn821Ile
XM_006712879.2:c.2381A>T XP_006712942.1:p.Asn794Ile
XM_006712880.2:c.2381A>T XP_006712943.1:p.Asn794Ile
XM_011512217.1:c.2534A>T XP_011510519.1:p.Asn845Ile
XM_011512218.1:c.2519A>T XP_011510520.1:p.Asn840Ile
XM_011512219.1:c.2504A>T XP_011510521.1:p.Asn835Ile
XM_011512220.1:c.2465A>T XP_011510522.1:p.Asn822Ile
XM_011512221.1:c.2462A>T XP_011510523.1:p.Asn821Ile
XM_011512222.1:c.2462A>T XP_011510524.1:p.Asn821Ile
XM_011512223.1:c.2462A>T XP_011510525.1:p.Asn821Ile
XM_011512224.1:c.2447A>T XP_011510526.1:p.Asn816Ile
XM_011512225.1:c.2432A>T XP_011510527.1:p.Asn811Ile
XM_011512226.1:c.2390A>T XP_011510528.1:p.Asn797Ile
XM_011512227.1:c.2318A>T XP_011510529.1:p.Asn773Ile
XM_011512228.1:c.2381A>T XP_011510530.1:p.Asn794Ile
XM_011512229.1:c.2381A>T XP_011510531.1:p.Asn794Ile
XM_011512230.1:c.1214A>T XP_011510532.1:p.Asn405Ile
XM_006712877.3:c.2519A>T XP_006712940.1:p.Asn840Ile
XM_006712878.3:c.2462A>T XP_006712941.1:p.Asn821Ile
XM_006712879.3:c.2381A>T XP_006712942.1:p.Asn794Ile
XM_006712880.3:c.2381A>T XP_006712943.1:p.Asn794Ile
XM_011512217.2:c.2534A>T XP_011510519.1:p.Asn845Ile
XM_011512218.2:c.2519A>T XP_011510520.1:p.Asn840Ile
XM_011512219.2:c.2504A>T XP_011510521.1:p.Asn835Ile
XM_011512220.2:c.2465A>T XP_011510522.1:p.Asn822Ile
XM_011512222.3:c.2462A>T XP_011510524.1:p.Asn821Ile
XM_011512223.2:c.2462A>T XP_011510525.1:p.Asn821Ile
XM_011512224.2:c.2447A>T XP_011510526.1:p.Asn816Ile
XM_011512225.2:c.2432A>T XP_011510527.1:p.Asn811Ile
XM_011512226.2:c.2390A>T XP_011510528.1:p.Asn797Ile
XM_011512227.2:c.2318A>T XP_011510529.1:p.Asn773Ile
XM_017005394.1:c.2402A>T XP_016860883.1:p.Asn801Ile
XM_017005395.1:c.1946A>T XP_016860884.1:p.Asn649Ile
XM_024453257.1:c.2381A>T XP_024309025.1:p.Asn794Ile
NM_001378414.1:c.2462A>T MANE Select NP_001365343.1:p.Asn821Ile
NM_001378415.1:c.2462A>T NP_001365344.1:p.Asn821Ile
NM_001378416.1:c.2447A>T NP_001365345.1:p.Asn816Ile
NM_001378417.1:c.2447A>T NP_001365346.1:p.Asn816Ile
NM_006037.4:c.2447A>T NP_006028.2:p.Asn816Ile