Canonical Allele Identifier: CA1043925714

Gene: HDAC4

Linked Data

• dbSNP Id: rs2037883416
• gnomAD v3: 2-239103895-A-G
• gnomAD v4: 2-239103895-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.239103895A>G , CM000664.2:g.239103895A>G	GRCh38
NC_000002.11:g.240025591A>G , CM000664.1:g.240025591A>G	GRCh37
NC_000002.10:g.239690528A>G	NCBI36
NG_009235.1:g.302053T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000543185.6:c.2113-999T>C MANE Select	ENSP00000440481.3:n.2113-999T>C
ENST00000345617.7:c.2098-999T>C	ENSP00000264606.3:n.2098-999T>C
ENST00000460235.1:n.56-999T>C
ENST00000463007.5:n.2550-999T>C
ENST00000487617.5:n.5-999T>C
ENST00000493582.5:n.2585-999T>C
ENST00000535493.5:n.2456-999T>C
ENST00000543185.5:c.1762-999T>C	ENSP00000440481.2:n.1762-999T>C
NM_006037.3:c.2098-999T>C	NP_006028.2:n.2098-999T>C
XM_006712877.2:c.2170-999T>C	XP_006712940.1:n.2170-999T>C
XM_006712878.2:c.2113-999T>C	XP_006712941.1:n.2113-999T>C
XM_006712879.2:c.2032-999T>C	XP_006712942.1:n.2032-999T>C
XM_006712880.2:c.2032-999T>C	XP_006712943.1:n.2032-999T>C
XM_011512217.1:c.2185-999T>C	XP_011510519.1:n.2185-999T>C
XM_011512218.1:c.2185-999T>C	XP_011510520.1:n.2185-999T>C
XM_011512219.1:c.2170-999T>C	XP_011510521.1:n.2170-999T>C
XM_011512220.1:c.2116-999T>C	XP_011510522.1:n.2116-999T>C
XM_011512221.1:c.2113-999T>C	XP_011510523.1:n.2113-999T>C
XM_011512222.1:c.2113-999T>C	XP_011510524.1:n.2113-999T>C
XM_011512223.1:c.2113-999T>C	XP_011510525.1:n.2113-999T>C
XM_011512224.1:c.2098-999T>C	XP_011510526.1:n.2098-999T>C
XM_011512225.1:c.2083-999T>C	XP_011510527.1:n.2083-999T>C
XM_011512226.1:c.2041-999T>C	XP_011510528.1:n.2041-999T>C
XM_011512227.1:c.1969-999T>C	XP_011510529.1:n.1969-999T>C
XM_011512228.1:c.2032-999T>C	XP_011510530.1:n.2032-999T>C
XM_011512229.1:c.2032-999T>C	XP_011510531.1:n.2032-999T>C
XM_011512230.1:c.865-999T>C	XP_011510532.1:n.865-999T>C
XM_006712877.3:c.2170-999T>C	XP_006712940.1:n.2170-999T>C
XM_006712878.3:c.2113-999T>C	XP_006712941.1:n.2113-999T>C
XM_006712879.3:c.2032-999T>C	XP_006712942.1:n.2032-999T>C
XM_006712880.3:c.2032-999T>C	XP_006712943.1:n.2032-999T>C
XM_011512217.2:c.2185-999T>C	XP_011510519.1:n.2185-999T>C
XM_011512218.2:c.2185-999T>C	XP_011510520.1:n.2185-999T>C
XM_011512219.2:c.2170-999T>C	XP_011510521.1:n.2170-999T>C
XM_011512220.2:c.2116-999T>C	XP_011510522.1:n.2116-999T>C
XM_011512222.3:c.2113-999T>C	XP_011510524.1:n.2113-999T>C
XM_011512223.2:c.2113-999T>C	XP_011510525.1:n.2113-999T>C
XM_011512224.2:c.2098-999T>C	XP_011510526.1:n.2098-999T>C
XM_011512225.2:c.2083-999T>C	XP_011510527.1:n.2083-999T>C
XM_011512226.2:c.2041-999T>C	XP_011510528.1:n.2041-999T>C
XM_011512227.2:c.1969-999T>C	XP_011510529.1:n.1969-999T>C
XM_017005394.1:c.2053-999T>C	XP_016860883.1:n.2053-999T>C
XM_017005395.1:c.1597-999T>C	XP_016860884.1:n.1597-999T>C
XM_024453257.1:c.2032-999T>C	XP_024309025.1:n.2032-999T>C
NM_001378414.1:c.2113-999T>C MANE Select	NP_001365343.1:n.2113-999T>C
NM_001378415.1:c.2113-999T>C	NP_001365344.1:n.2113-999T>C
NM_001378416.1:c.2098-999T>C	NP_001365345.1:n.2098-999T>C
NM_001378417.1:c.2098-999T>C	NP_001365346.1:n.2098-999T>C
NM_006037.4:c.2098-999T>C	NP_006028.2:n.2098-999T>C