Canonical Allele Identifier: CA2739278766

Gene: HDAC4

Linked Data

• ClinVar Variation Id: 2829628
• ClinVar RCV Id: RCV003694062

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.239082177del , CM000664.2:g.239082177del	GRCh38
NC_000002.11:g.240003873del , CM000664.1:g.240003873del	GRCh37
NC_000002.10:g.239668810del	NCBI36
NG_009235.1:g.323774del

Transcript Alleles

HGVS	Amino-acid change
ENST00000690129.1:n.594del
ENST00000543185.6:c.2580del MANE Select	ENSP00000440481.3:p.Ser861AlafsTer?
ENST00000345617.7:c.2565del	ENSP00000264606.3:p.Ser856AlafsTer?
ENST00000487617.5:n.472del
ENST00000543185.5:c.2229del	ENSP00000440481.2:p.Ser744AlafsTer?
NM_006037.3:c.2565del	NP_006028.2:p.Ser856AlafsTer?
XM_006712877.2:c.2637del	XP_006712940.1:p.Ser880AlafsTer?
XM_006712878.2:c.2580del	XP_006712941.1:p.Ser861AlafsTer?
XM_006712879.2:c.2499del	XP_006712942.1:p.Ser834AlafsTer?
XM_006712880.2:c.2499del	XP_006712943.1:p.Ser834AlafsTer?
XM_011512217.1:c.2652del	XP_011510519.1:p.Ser885AlafsTer?
XM_011512218.1:c.2637del	XP_011510520.1:p.Ser880AlafsTer?
XM_011512219.1:c.2622del	XP_011510521.1:p.Ser875AlafsTer?
XM_011512220.1:c.2583del	XP_011510522.1:p.Ser862AlafsTer?
XM_011512221.1:c.2580del	XP_011510523.1:p.Ser861AlafsTer?
XM_011512222.1:c.2580del	XP_011510524.1:p.Ser861AlafsTer?
XM_011512223.1:c.2580del	XP_011510525.1:p.Ser861AlafsTer?
XM_011512224.1:c.2565del	XP_011510526.1:p.Ser856AlafsTer?
XM_011512225.1:c.2550del	XP_011510527.1:p.Ser851AlafsTer?
XM_011512226.1:c.2508del	XP_011510528.1:p.Ser837AlafsTer?
XM_011512227.1:c.2436del	XP_011510529.1:p.Ser813AlafsTer?
XM_011512228.1:c.2499del	XP_011510530.1:p.Ser834AlafsTer?
XM_011512229.1:c.2499del	XP_011510531.1:p.Ser834AlafsTer?
XM_011512230.1:c.1332del	XP_011510532.1:p.Ser445AlafsTer?
XM_006712877.3:c.2637del	XP_006712940.1:p.Ser880AlafsTer?
XM_006712878.3:c.2580del	XP_006712941.1:p.Ser861AlafsTer?
XM_006712879.3:c.2499del	XP_006712942.1:p.Ser834AlafsTer?
XM_006712880.3:c.2499del	XP_006712943.1:p.Ser834AlafsTer?
XM_011512217.2:c.2652del	XP_011510519.1:p.Ser885AlafsTer?
XM_011512218.2:c.2637del	XP_011510520.1:p.Ser880AlafsTer?
XM_011512219.2:c.2622del	XP_011510521.1:p.Ser875AlafsTer?
XM_011512220.2:c.2583del	XP_011510522.1:p.Ser862AlafsTer?
XM_011512222.3:c.2580del	XP_011510524.1:p.Ser861AlafsTer?
XM_011512223.2:c.2580del	XP_011510525.1:p.Ser861AlafsTer?
XM_011512224.2:c.2565del	XP_011510526.1:p.Ser856AlafsTer?
XM_011512225.2:c.2550del	XP_011510527.1:p.Ser851AlafsTer?
XM_011512226.2:c.2508del	XP_011510528.1:p.Ser837AlafsTer?
XM_011512227.2:c.2436del	XP_011510529.1:p.Ser813AlafsTer?
XM_017005394.1:c.2520del	XP_016860883.1:p.Ser841AlafsTer?
XM_017005395.1:c.2064del	XP_016860884.1:p.Ser689AlafsTer?
XM_024453257.1:c.2499del	XP_024309025.1:p.Ser834AlafsTer?
NM_001378414.1:c.2580del MANE Select	NP_001365343.1:p.Ser861AlafsTer?
NM_001378415.1:c.2580del	NP_001365344.1:p.Ser861AlafsTer?
NM_001378416.1:c.2565del	NP_001365345.1:p.Ser856AlafsTer?
NM_001378417.1:c.2565del	NP_001365346.1:p.Ser856AlafsTer?
NM_006037.4:c.2565del	NP_006028.2:p.Ser856AlafsTer?