Canonical Allele Identifier: CA2579644995
Community Standard Title: NM_018486.3(HDAC8):c.1112-11C>G
Gene: HDAC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.72330087G>C , CM000685.2:g.72330087G>C GRCh38
NC_000023.10:g.71549937G>C , CM000685.1:g.71549937G>C GRCh37
NC_000023.9:g.71466662G>C NCBI36
NG_015851.1:g.248017C>G

Transcript Alleles

HGVS Amino-acid Change
NM_018486.3:c.1112-11C>G MANE Select NP_060956.1:n.1112-11C>G
ENST00000373573.9:c.1112-11C>G MANE Select ENSP00000362674.3:n.1112-11C>G
NM_001166418.1:c.839-11C>G NP_001159890.1:n.839-11C>G
NM_001166418.2:c.839-11C>G NP_001159890.1:n.839-11C>G
NM_018486.2:c.1112-11C>G NP_060956.1:n.1112-11C>G
NR_051952.1:n.1312-11C>G
NR_051952.2:n.1052-11C>G
ENST00000373573.7:c.1112-11C>G ENSP00000362674.3:n.1112-11C>G
ENST00000373583.5:c.165-378C>G ENSP00000362685.1:n.165-378C>G
ENST00000373583.6:c.1034-11C>G ENSP00000362685.2:n.1034-11C>G
ENST00000373589.8:c.839-11C>G ENSP00000362691.4:n.839-11C>G
ENST00000373589.9:c.839-11C>G ENSP00000362691.4:n.839-11C>G
ENST00000647594.1:c.*51-11C>G ENSP00000496814.1:n.*51-11C>G
ENST00000647613.1:c.*864+21646C>G ENSP00000497911.1:n.*864+21646C>G
ENST00000647654.1:c.917-11C>G ENSP00000497568.1:n.917-11C>G
ENST00000647859.1:c.*779C>G ENSP00000497530.1:n.*779C>G
ENST00000647886.1:c.1190-11C>G ENSP00000497188.1:n.1190-11C>G
ENST00000647980.1:c.1106-11C>G ENSP00000498002.1:n.1106-11C>G
ENST00000648276.1:c.496-11C>G ENSP00000497619.1:n.496-11C>G
ENST00000648452.1:c.1223-11C>G ENSP00000497268.1:n.1223-11C>G
ENST00000648459.1:c.509-11C>G ENSP00000498072.1:n.509-11C>G
ENST00000648504.1:c.1239-11C>G ENSP00000497668.1:n.1239-11C>G
ENST00000648731.1:c.1218-11C>G
ENST00000648850.1:c.751-11C>G
ENST00000648855.1:n.1222-11C>G
ENST00000648922.1:c.1111+21646C>G ENSP00000497072.1:n.1111+21646C>G
ENST00000648939.1:c.*192-11C>G ENSP00000497442.1:n.*192-11C>G
ENST00000649097.1:c.*219-11C>G ENSP00000497551.1:n.*219-11C>G
ENST00000649181.1:c.*474-11C>G ENSP00000498150.1:n.*474-11C>G
ENST00000649274.1:c.1128-11C>G ENSP00000497032.1:n.1128-11C>G
ENST00000650076.1:c.469-11C>G
ENST00000650471.1:c.*556-11C>G ENSP00000498027.1:n.*556-11C>G
ENST00000650477.1:n.168-11C>G
ENST00000650604.1:c.539-11C>G ENSP00000497105.1:n.539-11C>G
XM_011530986.1:c.1190-11C>G XP_011529288.1:n.1190-11C>G
XM_011530986.3:c.1190-11C>G XP_011529288.3:n.1190-11C>G
XM_017029640.2:c.1112-11C>G XP_016885129.2:n.1112-11C>G
XM_017029641.2:c.1034-11C>G XP_016885130.2:n.1034-11C>G
XM_017029642.1:c.1031-11C>G XP_016885131.1:n.1031-11C>G
XM_017029643.2:c.1004-11C>G XP_016885132.1:n.1004-11C>G
XM_017029644.2:c.953-11C>G XP_016885133.1:n.953-11C>G
XM_017029645.2:c.926-11C>G XP_016885134.1:n.926-11C>G
XM_017029646.1:c.803-11C>G XP_016885135.1:n.803-11C>G
XM_024452405.1:c.605-11C>G XP_024308173.1:n.605-11C>G
XR_001755711.2:n.1384-11C>G
XR_002958780.1:n.1202-11C>G
XR_002958781.1:n.1388-11C>G
XR_938402.1:n.1259-11C>G
XR_938402.3:n.1259-11C>G