Canonical Allele Identifier: CA351261750

Gene: HDAC4

Linked Data

• dbSNP Id: rs2035636562
• gnomAD v3: 2-239084204-T-G
• gnomAD v4: 2-239084204-T-G
• MyVariant Identifiers: chr2:g.240005900T>G (hg19) ; chr2:g.239084204T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.239084204T>G , CM000664.2:g.239084204T>G	GRCh38
NC_000002.11:g.240005900T>G , CM000664.1:g.240005900T>G	GRCh37
NC_000002.10:g.239670837T>G	NCBI36
NG_009235.1:g.321744A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690129.1:n.497A>C
ENST00000543185.6:c.2483A>C MANE Select	ENSP00000440481.3:p.Lys828Thr
ENST00000345617.7:c.2468A>C	ENSP00000264606.3:p.Lys823Thr
ENST00000487617.5:n.375A>C
ENST00000543185.5:c.2132A>C	ENSP00000440481.2:p.Lys711Thr
NM_006037.3:c.2468A>C	NP_006028.2:p.Lys823Thr
XM_006712877.2:c.2540A>C	XP_006712940.1:p.Lys847Thr
XM_006712878.2:c.2483A>C	XP_006712941.1:p.Lys828Thr
XM_006712879.2:c.2402A>C	XP_006712942.1:p.Lys801Thr
XM_006712880.2:c.2402A>C	XP_006712943.1:p.Lys801Thr
XM_011512217.1:c.2555A>C	XP_011510519.1:p.Lys852Thr
XM_011512218.1:c.2540A>C	XP_011510520.1:p.Lys847Thr
XM_011512219.1:c.2525A>C	XP_011510521.1:p.Lys842Thr
XM_011512220.1:c.2486A>C	XP_011510522.1:p.Lys829Thr
XM_011512221.1:c.2483A>C	XP_011510523.1:p.Lys828Thr
XM_011512222.1:c.2483A>C	XP_011510524.1:p.Lys828Thr
XM_011512223.1:c.2483A>C	XP_011510525.1:p.Lys828Thr
XM_011512224.1:c.2468A>C	XP_011510526.1:p.Lys823Thr
XM_011512225.1:c.2453A>C	XP_011510527.1:p.Lys818Thr
XM_011512226.1:c.2411A>C	XP_011510528.1:p.Lys804Thr
XM_011512227.1:c.2339A>C	XP_011510529.1:p.Lys780Thr
XM_011512228.1:c.2402A>C	XP_011510530.1:p.Lys801Thr
XM_011512229.1:c.2402A>C	XP_011510531.1:p.Lys801Thr
XM_011512230.1:c.1235A>C	XP_011510532.1:p.Lys412Thr
XM_006712877.3:c.2540A>C	XP_006712940.1:p.Lys847Thr
XM_006712878.3:c.2483A>C	XP_006712941.1:p.Lys828Thr
XM_006712879.3:c.2402A>C	XP_006712942.1:p.Lys801Thr
XM_006712880.3:c.2402A>C	XP_006712943.1:p.Lys801Thr
XM_011512217.2:c.2555A>C	XP_011510519.1:p.Lys852Thr
XM_011512218.2:c.2540A>C	XP_011510520.1:p.Lys847Thr
XM_011512219.2:c.2525A>C	XP_011510521.1:p.Lys842Thr
XM_011512220.2:c.2486A>C	XP_011510522.1:p.Lys829Thr
XM_011512222.3:c.2483A>C	XP_011510524.1:p.Lys828Thr
XM_011512223.2:c.2483A>C	XP_011510525.1:p.Lys828Thr
XM_011512224.2:c.2468A>C	XP_011510526.1:p.Lys823Thr
XM_011512225.2:c.2453A>C	XP_011510527.1:p.Lys818Thr
XM_011512226.2:c.2411A>C	XP_011510528.1:p.Lys804Thr
XM_011512227.2:c.2339A>C	XP_011510529.1:p.Lys780Thr
XM_017005394.1:c.2423A>C	XP_016860883.1:p.Lys808Thr
XM_017005395.1:c.1967A>C	XP_016860884.1:p.Lys656Thr
XM_024453257.1:c.2402A>C	XP_024309025.1:p.Lys801Thr
NM_001378414.1:c.2483A>C MANE Select	NP_001365343.1:p.Lys828Thr
NM_001378415.1:c.2483A>C	NP_001365344.1:p.Lys828Thr
NM_001378416.1:c.2468A>C	NP_001365345.1:p.Lys823Thr
NM_001378417.1:c.2468A>C	NP_001365346.1:p.Lys823Thr
NM_006037.4:c.2468A>C	NP_006028.2:p.Lys823Thr