Canonical Allele Identifier: CA351261914

Gene: HDAC4

Linked Data

• MyVariant Identifiers: chr2:g.240005924A>T (hg19) ; chr2:g.239084228A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.239084228A>T , CM000664.2:g.239084228A>T	GRCh38
NC_000002.11:g.240005924A>T , CM000664.1:g.240005924A>T	GRCh37
NC_000002.10:g.239670861A>T	NCBI36
NG_009235.1:g.321720T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690129.1:n.473T>A
ENST00000543185.6:c.2459T>A MANE Select	ENSP00000440481.3:p.Phe820Tyr
ENST00000345617.7:c.2444T>A	ENSP00000264606.3:p.Phe815Tyr
ENST00000487617.5:n.351T>A
ENST00000543185.5:c.2108T>A	ENSP00000440481.2:p.Phe703Tyr
NM_006037.3:c.2444T>A	NP_006028.2:p.Phe815Tyr
XM_006712877.2:c.2516T>A	XP_006712940.1:p.Phe839Tyr
XM_006712878.2:c.2459T>A	XP_006712941.1:p.Phe820Tyr
XM_006712879.2:c.2378T>A	XP_006712942.1:p.Phe793Tyr
XM_006712880.2:c.2378T>A	XP_006712943.1:p.Phe793Tyr
XM_011512217.1:c.2531T>A	XP_011510519.1:p.Phe844Tyr
XM_011512218.1:c.2516T>A	XP_011510520.1:p.Phe839Tyr
XM_011512219.1:c.2501T>A	XP_011510521.1:p.Phe834Tyr
XM_011512220.1:c.2462T>A	XP_011510522.1:p.Phe821Tyr
XM_011512221.1:c.2459T>A	XP_011510523.1:p.Phe820Tyr
XM_011512222.1:c.2459T>A	XP_011510524.1:p.Phe820Tyr
XM_011512223.1:c.2459T>A	XP_011510525.1:p.Phe820Tyr
XM_011512224.1:c.2444T>A	XP_011510526.1:p.Phe815Tyr
XM_011512225.1:c.2429T>A	XP_011510527.1:p.Phe810Tyr
XM_011512226.1:c.2387T>A	XP_011510528.1:p.Phe796Tyr
XM_011512227.1:c.2315T>A	XP_011510529.1:p.Phe772Tyr
XM_011512228.1:c.2378T>A	XP_011510530.1:p.Phe793Tyr
XM_011512229.1:c.2378T>A	XP_011510531.1:p.Phe793Tyr
XM_011512230.1:c.1211T>A	XP_011510532.1:p.Phe404Tyr
XM_006712877.3:c.2516T>A	XP_006712940.1:p.Phe839Tyr
XM_006712878.3:c.2459T>A	XP_006712941.1:p.Phe820Tyr
XM_006712879.3:c.2378T>A	XP_006712942.1:p.Phe793Tyr
XM_006712880.3:c.2378T>A	XP_006712943.1:p.Phe793Tyr
XM_011512217.2:c.2531T>A	XP_011510519.1:p.Phe844Tyr
XM_011512218.2:c.2516T>A	XP_011510520.1:p.Phe839Tyr
XM_011512219.2:c.2501T>A	XP_011510521.1:p.Phe834Tyr
XM_011512220.2:c.2462T>A	XP_011510522.1:p.Phe821Tyr
XM_011512222.3:c.2459T>A	XP_011510524.1:p.Phe820Tyr
XM_011512223.2:c.2459T>A	XP_011510525.1:p.Phe820Tyr
XM_011512224.2:c.2444T>A	XP_011510526.1:p.Phe815Tyr
XM_011512225.2:c.2429T>A	XP_011510527.1:p.Phe810Tyr
XM_011512226.2:c.2387T>A	XP_011510528.1:p.Phe796Tyr
XM_011512227.2:c.2315T>A	XP_011510529.1:p.Phe772Tyr
XM_017005394.1:c.2399T>A	XP_016860883.1:p.Phe800Tyr
XM_017005395.1:c.1943T>A	XP_016860884.1:p.Phe648Tyr
XM_024453257.1:c.2378T>A	XP_024309025.1:p.Phe793Tyr
NM_001378414.1:c.2459T>A MANE Select	NP_001365343.1:p.Phe820Tyr
NM_001378415.1:c.2459T>A	NP_001365344.1:p.Phe820Tyr
NM_001378416.1:c.2444T>A	NP_001365345.1:p.Phe815Tyr
NM_001378417.1:c.2444T>A	NP_001365346.1:p.Phe815Tyr
NM_006037.4:c.2444T>A	NP_006028.2:p.Phe815Tyr