Canonical Allele Identifier: CA2322832101
Gene: DOCK6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11232382T= , CM000681.2:g.11232382T= GRCh38
NC_000019.9:g.11343058T= , CM000681.1:g.11343058T= GRCh37
NC_000019.8:g.11204058T= NCBI36
NG_031953.1:g.35111A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000587656.6:c.2719-93A= ENSP00000468638.2:n.2719-93A=
ENST00000294618.12:c.2718+821A= MANE Select ENSP00000294618.6:n.2718+821A=
ENST00000294618.11:c.2718+821A= ENSP00000294618.6:n.2718+821A=
ENST00000585904.1:c.322-93A= ENSP00000465767.1:n.322-93A=
ENST00000587656.5:c.479-93A=
ENST00000590680.5:c.1061+821A=
NM_020812.3:c.2718+821A= NP_065863.2:n.2718+821A=
XM_005260000.2:c.2719-93A= XP_005260057.1:n.2719-93A=
XM_005260001.2:c.2719-93A= XP_005260058.1:n.2719-93A=
XM_006722804.2:c.54+657A= XP_006722867.1:n.54+657A=
XM_011528150.1:c.2752-93A= XP_011526452.1:n.2752-93A=
XM_011528151.1:c.2751+821A= XP_011526453.1:n.2751+821A=
XM_011528152.1:c.2751+821A= XP_011526454.1:n.2751+821A=
XM_011528153.1:c.2752-93A= XP_011526455.1:n.2752-93A=
XR_936195.1:n.2813-93A=
XR_936196.1:n.2812+821A=
XR_936197.1:n.2813-93A=
XR_936198.1:n.2812+821A=
XM_006722804.3:c.54+657A= XP_006722867.1:n.54+657A=
NM_001367830.1:c.2719-93A= NP_001354759.1:n.2719-93A=
NM_020812.4:c.2718+821A= MANE Select NP_065863.2:n.2718+821A=