Canonical Allele Identifier: CA431978659

Gene: HDAC4

Linked Data

• MyVariant Identifiers: chr2:g.240005857C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.239084161C>A , CM000664.2:g.239084161C>A	GRCh38
NC_000002.11:g.240005857C>A , CM000664.1:g.240005857C>A	GRCh37
NC_000002.10:g.239670794C>A	NCBI36
NG_009235.1:g.321787G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690129.1:n.540G>T
ENST00000543185.6:c.2526G>T MANE Select	ENSP00000440481.3:p.Val842=
ENST00000345617.7:c.2511G>T	ENSP00000264606.3:p.Val837=
ENST00000487617.5:n.418G>T
ENST00000543185.5:c.2175G>T	ENSP00000440481.2:p.Val725=
NM_006037.3:c.2511G>T	NP_006028.2:p.Val837=
XM_006712877.2:c.2583G>T	XP_006712940.1:p.Val861=
XM_006712878.2:c.2526G>T	XP_006712941.1:p.Val842=
XM_006712879.2:c.2445G>T	XP_006712942.1:p.Val815=
XM_006712880.2:c.2445G>T	XP_006712943.1:p.Val815=
XM_011512217.1:c.2598G>T	XP_011510519.1:p.Val866=
XM_011512218.1:c.2583G>T	XP_011510520.1:p.Val861=
XM_011512219.1:c.2568G>T	XP_011510521.1:p.Val856=
XM_011512220.1:c.2529G>T	XP_011510522.1:p.Val843=
XM_011512221.1:c.2526G>T	XP_011510523.1:p.Val842=
XM_011512222.1:c.2526G>T	XP_011510524.1:p.Val842=
XM_011512223.1:c.2526G>T	XP_011510525.1:p.Val842=
XM_011512224.1:c.2511G>T	XP_011510526.1:p.Val837=
XM_011512225.1:c.2496G>T	XP_011510527.1:p.Val832=
XM_011512226.1:c.2454G>T	XP_011510528.1:p.Val818=
XM_011512227.1:c.2382G>T	XP_011510529.1:p.Val794=
XM_011512228.1:c.2445G>T	XP_011510530.1:p.Val815=
XM_011512229.1:c.2445G>T	XP_011510531.1:p.Val815=
XM_011512230.1:c.1278G>T	XP_011510532.1:p.Val426=
XM_006712877.3:c.2583G>T	XP_006712940.1:p.Val861=
XM_006712878.3:c.2526G>T	XP_006712941.1:p.Val842=
XM_006712879.3:c.2445G>T	XP_006712942.1:p.Val815=
XM_006712880.3:c.2445G>T	XP_006712943.1:p.Val815=
XM_011512217.2:c.2598G>T	XP_011510519.1:p.Val866=
XM_011512218.2:c.2583G>T	XP_011510520.1:p.Val861=
XM_011512219.2:c.2568G>T	XP_011510521.1:p.Val856=
XM_011512220.2:c.2529G>T	XP_011510522.1:p.Val843=
XM_011512222.3:c.2526G>T	XP_011510524.1:p.Val842=
XM_011512223.2:c.2526G>T	XP_011510525.1:p.Val842=
XM_011512224.2:c.2511G>T	XP_011510526.1:p.Val837=
XM_011512225.2:c.2496G>T	XP_011510527.1:p.Val832=
XM_011512226.2:c.2454G>T	XP_011510528.1:p.Val818=
XM_011512227.2:c.2382G>T	XP_011510529.1:p.Val794=
XM_017005394.1:c.2466G>T	XP_016860883.1:p.Val822=
XM_017005395.1:c.2010G>T	XP_016860884.1:p.Val670=
XM_024453257.1:c.2445G>T	XP_024309025.1:p.Val815=
NM_001378414.1:c.2526G>T MANE Select	NP_001365343.1:p.Val842=
NM_001378415.1:c.2526G>T	NP_001365344.1:p.Val842=
NM_001378416.1:c.2511G>T	NP_001365345.1:p.Val837=
NM_001378417.1:c.2511G>T	NP_001365346.1:p.Val837=
NM_006037.4:c.2511G>T	NP_006028.2:p.Val837=