Canonical Allele Identifier: CA2322832007
Gene: DOCK6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11232236A= , CM000681.2:g.11232236A= GRCh38
NC_000019.9:g.11342912A= , CM000681.1:g.11342912A= GRCh37
NC_000019.8:g.11203912A= NCBI36
NG_031953.1:g.35257T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000587656.6:c.2772T= ENSP00000468638.2:p.Ser924=
ENST00000294618.12:c.2718+967T= MANE Select ENSP00000294618.6:n.2718+967T=
ENST00000294618.11:c.2718+967T= ENSP00000294618.6:n.2718+967T=
ENST00000585904.1:c.375T= ENSP00000465767.1:p.Ser125=
ENST00000587656.5:c.532T=
ENST00000590680.5:c.1061+967T=
NM_020812.3:c.2718+967T= NP_065863.2:n.2718+967T=
XM_005260000.2:c.2772T= XP_005260057.1:p.Ser924=
XM_005260001.2:c.2772T= XP_005260058.1:p.Ser924=
XM_006722804.2:c.54+803T= XP_006722867.1:n.54+803T=
XM_011528150.1:c.2805T= XP_011526452.1:p.Ser935=
XM_011528151.1:c.2751+967T= XP_011526453.1:n.2751+967T=
XM_011528152.1:c.2751+967T= XP_011526454.1:n.2751+967T=
XM_011528153.1:c.2805T= XP_011526455.1:p.Ser935=
XR_936195.1:n.2866T=
XR_936196.1:n.2812+967T=
XR_936197.1:n.2866T=
XR_936198.1:n.2812+967T=
XM_006722804.3:c.54+803T= XP_006722867.1:n.54+803T=
NM_001367830.1:c.2772T= NP_001354759.1:p.Ser924=
NM_020812.4:c.2718+967T= MANE Select NP_065863.2:n.2718+967T=