Canonical Allele Identifier: CA2322832026
Gene: DOCK6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11232275T= , CM000681.2:g.11232275T= GRCh38
NC_000019.9:g.11342951T= , CM000681.1:g.11342951T= GRCh37
NC_000019.8:g.11203951T= NCBI36
NG_031953.1:g.35218A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000587656.6:c.2733A= ENSP00000468638.2:p.Ser911=
ENST00000294618.12:c.2718+928A= MANE Select ENSP00000294618.6:n.2718+928A=
ENST00000294618.11:c.2718+928A= ENSP00000294618.6:n.2718+928A=
ENST00000585904.1:c.336A= ENSP00000465767.1:p.Ser112=
ENST00000587656.5:c.493A=
ENST00000590680.5:c.1061+928A=
NM_020812.3:c.2718+928A= NP_065863.2:n.2718+928A=
XM_005260000.2:c.2733A= XP_005260057.1:p.Ser911=
XM_005260001.2:c.2733A= XP_005260058.1:p.Ser911=
XM_006722804.2:c.54+764A= XP_006722867.1:n.54+764A=
XM_011528150.1:c.2766A= XP_011526452.1:p.Ser922=
XM_011528151.1:c.2751+928A= XP_011526453.1:n.2751+928A=
XM_011528152.1:c.2751+928A= XP_011526454.1:n.2751+928A=
XM_011528153.1:c.2766A= XP_011526455.1:p.Ser922=
XR_936195.1:n.2827A=
XR_936196.1:n.2812+928A=
XR_936197.1:n.2827A=
XR_936198.1:n.2812+928A=
XM_006722804.3:c.54+764A= XP_006722867.1:n.54+764A=
NM_001367830.1:c.2733A= NP_001354759.1:p.Ser911=
NM_020812.4:c.2718+928A= MANE Select NP_065863.2:n.2718+928A=