Canonical Allele Identifier: CA413643048

Gene: HDAC8

Linked Data

• MyVariant Identifiers: chrX:g.71684490A>C (hg19) ; chrX:g.72464640A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.72464640A>C , CM000685.2:g.72464640A>C	GRCh38
NC_000023.10:g.71684490A>C , CM000685.1:g.71684490A>C	GRCh37
NC_000023.9:g.71601215A>C	NCBI36
NG_015851.1:g.113464T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000373568.7:c.829T>G	ENSP00000362669.3:p.Phe277Val
ENST00000373573.9:c.829T>G MANE Select	ENSP00000362674.3:p.Phe277Val
ENST00000373583.6:c.751T>G	ENSP00000362685.2:p.Phe251Val
ENST00000373589.9:c.556T>G	ENSP00000362691.4:p.Phe186Val
ENST00000415409.6:c.829T>G	ENSP00000396424.2:p.Phe277Val
ENST00000436675.6:c.*84T>G	ENSP00000416489.1:n.*84T>G
ENST00000478743.2:n.915T>G
ENST00000647594.1:c.829T>G	ENSP00000496814.1:p.Phe277Val
ENST00000647606.1:c.604T>G
ENST00000647613.1:c.*582T>G	ENSP00000497911.1:n.*582T>G
ENST00000647641.1:n.916T>G
ENST00000647654.1:c.556T>G	ENSP00000497568.1:p.Phe186Val
ENST00000647718.1:n.884T>G
ENST00000647859.1:c.829T>G	ENSP00000497530.1:p.Phe277Val
ENST00000647886.1:c.829T>G	ENSP00000497188.1:p.Phe277Val
ENST00000647980.1:c.823T>G	ENSP00000498002.1:p.Phe275Val
ENST00000648139.1:c.529T>G	ENSP00000496818.1:p.Phe177Val
ENST00000648276.1:c.73T>G	ENSP00000497619.1:p.Phe25Val
ENST00000648285.1:n.612T>G
ENST00000648298.1:c.829T>G	ENSP00000496866.1:p.Phe277Val
ENST00000648452.1:c.829T>G	ENSP00000497268.1:p.Phe277Val
ENST00000648459.1:c.226T>G	ENSP00000498072.1:p.Phe76Val
ENST00000648504.1:c.766T>G	ENSP00000497668.1:p.Phe256Val
ENST00000648711.1:c.454T>G	ENSP00000498040.1:p.Phe152Val
ENST00000648731.1:c.935T>G
ENST00000648834.1:c.829T>G	ENSP00000497764.1:p.Phe277Val
ENST00000648850.1:c.464T>G
ENST00000648855.1:n.753T>G
ENST00000648870.1:c.829T>G	ENSP00000497599.1:p.Phe277Val
ENST00000648922.1:c.829T>G	ENSP00000497072.1:p.Phe277Val
ENST00000648939.1:c.829T>G	ENSP00000497442.1:p.Phe277Val
ENST00000649097.1:c.829T>G	ENSP00000497551.1:p.Phe277Val
ENST00000649116.1:c.*386T>G	ENSP00000497925.1:n.*386T>G
ENST00000649181.1:c.*191T>G	ENSP00000498150.1:n.*191T>G
ENST00000649242.1:c.*433T>G	ENSP00000497943.1:n.*433T>G
ENST00000649274.1:c.767T>G	ENSP00000497032.1:n.767T>G
ENST00000649518.1:c.*433T>G	ENSP00000498169.1:n.*433T>G
ENST00000649543.1:c.*433T>G	ENSP00000496826.1:n.*433T>G
ENST00000649752.1:c.556T>G	ENSP00000497267.1:p.Phe186Val
ENST00000650076.1:c.211+24293T>G
ENST00000650471.1:c.*273T>G	ENSP00000498027.1:n.*273T>G
ENST00000650604.1:c.256T>G	ENSP00000497105.1:p.Phe86Val
ENST00000373568.6:c.556T>G	ENSP00000362669.2:p.Phe186Val
ENST00000373573.7:c.829T>G	ENSP00000362674.3:p.Phe277Val
ENST00000373583.5:c.164+107417T>G	ENSP00000362685.1:n.164+107417T>G
ENST00000373589.8:c.556T>G	ENSP00000362691.4:p.Phe186Val
ENST00000415409.5:c.751T>G	ENSP00000396424.1:p.Phe251Val
ENST00000436675.5:c.*84T>G	ENSP00000416489.1:n.*84T>G
NM_001166418.1:c.556T>G	NP_001159890.1:p.Phe186Val
NM_018486.2:c.829T>G	NP_060956.1:p.Phe277Val
NR_051952.1:n.1029T>G
XM_011530986.1:c.829T>G	XP_011529288.1:p.Phe277Val
XM_011530987.1:c.829T>G	XP_011529289.1:p.Phe277Val
XM_011530988.1:c.829T>G	XP_011529290.1:p.Phe277Val
XR_938402.1:n.915T>G
XM_011530986.3:c.829T>G	XP_011529288.3:p.Phe277Val
XM_017029640.2:c.751T>G	XP_016885129.2:p.Phe251Val
XM_017029641.2:c.751T>G	XP_016885130.2:p.Phe251Val
XM_017029642.1:c.670T>G	XP_016885131.1:p.Phe224Val
XM_017029643.2:c.643T>G	XP_016885132.1:p.Phe215Val
XM_017029644.2:c.592T>G	XP_016885133.1:p.Phe198Val
XM_017029645.2:c.643T>G	XP_016885134.1:p.Phe215Val
XM_017029646.1:c.442T>G	XP_016885135.1:p.Phe148Val
XM_024452405.1:c.244T>G	XP_024308173.1:p.Phe82Val
XR_001755711.2:n.915T>G
XR_002958779.1:n.915T>G
XR_002958780.1:n.915T>G
XR_002958781.1:n.915T>G
XR_002958782.1:n.891T>G
XR_002958783.1:n.891T>G
XR_938402.3:n.915T>G
NM_018486.3:c.829T>G MANE Select	NP_060956.1:p.Phe277Val
NM_001166418.2:c.556T>G	NP_001159890.1:p.Phe186Val
NR_051952.2:n.769T>G