Canonical Allele Identifier: CA351261399

Gene: HDAC4

Linked Data

• MyVariant Identifiers: chr2:g.240005853A>G (hg19) ; chr2:g.239084157A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.239084157A>G , CM000664.2:g.239084157A>G	GRCh38
NC_000002.11:g.240005853A>G , CM000664.1:g.240005853A>G	GRCh37
NC_000002.10:g.239670790A>G	NCBI36
NG_009235.1:g.321791T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690129.1:n.544T>C
ENST00000543185.6:c.2530T>C MANE Select	ENSP00000440481.3:p.Trp844Arg
ENST00000345617.7:c.2515T>C	ENSP00000264606.3:p.Trp839Arg
ENST00000487617.5:n.422T>C
ENST00000543185.5:c.2179T>C	ENSP00000440481.2:p.Trp727Arg
NM_006037.3:c.2515T>C	NP_006028.2:p.Trp839Arg
XM_006712877.2:c.2587T>C	XP_006712940.1:p.Trp863Arg
XM_006712878.2:c.2530T>C	XP_006712941.1:p.Trp844Arg
XM_006712879.2:c.2449T>C	XP_006712942.1:p.Trp817Arg
XM_006712880.2:c.2449T>C	XP_006712943.1:p.Trp817Arg
XM_011512217.1:c.2602T>C	XP_011510519.1:p.Trp868Arg
XM_011512218.1:c.2587T>C	XP_011510520.1:p.Trp863Arg
XM_011512219.1:c.2572T>C	XP_011510521.1:p.Trp858Arg
XM_011512220.1:c.2533T>C	XP_011510522.1:p.Trp845Arg
XM_011512221.1:c.2530T>C	XP_011510523.1:p.Trp844Arg
XM_011512222.1:c.2530T>C	XP_011510524.1:p.Trp844Arg
XM_011512223.1:c.2530T>C	XP_011510525.1:p.Trp844Arg
XM_011512224.1:c.2515T>C	XP_011510526.1:p.Trp839Arg
XM_011512225.1:c.2500T>C	XP_011510527.1:p.Trp834Arg
XM_011512226.1:c.2458T>C	XP_011510528.1:p.Trp820Arg
XM_011512227.1:c.2386T>C	XP_011510529.1:p.Trp796Arg
XM_011512228.1:c.2449T>C	XP_011510530.1:p.Trp817Arg
XM_011512229.1:c.2449T>C	XP_011510531.1:p.Trp817Arg
XM_011512230.1:c.1282T>C	XP_011510532.1:p.Trp428Arg
XM_006712877.3:c.2587T>C	XP_006712940.1:p.Trp863Arg
XM_006712878.3:c.2530T>C	XP_006712941.1:p.Trp844Arg
XM_006712879.3:c.2449T>C	XP_006712942.1:p.Trp817Arg
XM_006712880.3:c.2449T>C	XP_006712943.1:p.Trp817Arg
XM_011512217.2:c.2602T>C	XP_011510519.1:p.Trp868Arg
XM_011512218.2:c.2587T>C	XP_011510520.1:p.Trp863Arg
XM_011512219.2:c.2572T>C	XP_011510521.1:p.Trp858Arg
XM_011512220.2:c.2533T>C	XP_011510522.1:p.Trp845Arg
XM_011512222.3:c.2530T>C	XP_011510524.1:p.Trp844Arg
XM_011512223.2:c.2530T>C	XP_011510525.1:p.Trp844Arg
XM_011512224.2:c.2515T>C	XP_011510526.1:p.Trp839Arg
XM_011512225.2:c.2500T>C	XP_011510527.1:p.Trp834Arg
XM_011512226.2:c.2458T>C	XP_011510528.1:p.Trp820Arg
XM_011512227.2:c.2386T>C	XP_011510529.1:p.Trp796Arg
XM_017005394.1:c.2470T>C	XP_016860883.1:p.Trp824Arg
XM_017005395.1:c.2014T>C	XP_016860884.1:p.Trp672Arg
XM_024453257.1:c.2449T>C	XP_024309025.1:p.Trp817Arg
NM_001378414.1:c.2530T>C MANE Select	NP_001365343.1:p.Trp844Arg
NM_001378415.1:c.2530T>C	NP_001365344.1:p.Trp844Arg
NM_001378416.1:c.2515T>C	NP_001365345.1:p.Trp839Arg
NM_001378417.1:c.2515T>C	NP_001365346.1:p.Trp839Arg
NM_006037.4:c.2515T>C	NP_006028.2:p.Trp839Arg