Canonical Allele Identifier: CA9207201

Gene: DOCK6

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11217380G>A , CM000681.2:g.11217380G>A	GRCh38
NC_000019.9:g.11328056G>A , CM000681.1:g.11328056G>A	GRCh37
NC_000019.8:g.11189056G>A	NCBI36
NG_031953.1:g.50113C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587656.6:c.3667C>T	ENSP00000468638.2:p.Gln1223Ter
ENST00000294618.12:c.3562C>T MANE Select	ENSP00000294618.6:p.Gln1188Ter
ENST00000294618.11:c.3562C>T	ENSP00000294618.6:p.Gln1188Ter
ENST00000587656.5:c.1427C>T
NM_020812.3:c.3562C>T	NP_065863.2:p.Gln1188Ter
XM_005260000.2:c.3760C>T	XP_005260057.1:p.Gln1254Ter
XM_005260001.2:c.3667C>T	XP_005260058.1:p.Gln1223Ter
XM_006722804.2:c.898C>T	XP_006722867.1:p.Gln300Ter
XM_011528150.1:c.3700C>T	XP_011526452.1:p.Gln1234Ter
XM_011528151.1:c.3688C>T	XP_011526453.1:p.Gln1230Ter
XM_011528152.1:c.3595C>T	XP_011526454.1:p.Gln1199Ter
XM_011528153.1:c.3700C>T	XP_011526455.1:p.Gln1234Ter
XR_936195.1:n.3761C>T
XR_936196.1:n.3778C>T
XM_006722804.3:c.898C>T	XP_006722867.1:p.Gln300Ter
NM_001367830.1:c.3667C>T	NP_001354759.1:p.Gln1223Ter
NM_020812.4:c.3562C>T MANE Select	NP_065863.2:p.Gln1188Ter