Canonical Allele Identifier: CA2813601517
Gene: DOCK6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11232120G>A , CM000681.2:g.11232120G>A GRCh38
NC_000019.9:g.11342796G>A , CM000681.1:g.11342796G>A GRCh37
NC_000019.8:g.11203796G>A NCBI36
NG_031953.1:g.35373C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000587656.6:c.2823+65C>T ENSP00000468638.2:n.2823+65C>T
ENST00000294618.12:c.2718+1083C>T MANE Select ENSP00000294618.6:n.2718+1083C>T
ENST00000294618.11:c.2718+1083C>T ENSP00000294618.6:n.2718+1083C>T
ENST00000585904.1:c.426+65C>T ENSP00000465767.1:n.426+65C>T
ENST00000587656.5:c.583+65C>T
ENST00000590680.5:c.1061+1083C>T
NM_020812.3:c.2718+1083C>T NP_065863.2:n.2718+1083C>T
XM_005260000.2:c.2823+65C>T XP_005260057.1:n.2823+65C>T
XM_005260001.2:c.2823+65C>T XP_005260058.1:n.2823+65C>T
XM_006722804.2:c.54+919C>T XP_006722867.1:n.54+919C>T
XM_011528150.1:c.2856+65C>T XP_011526452.1:n.2856+65C>T
XM_011528151.1:c.2751+1083C>T XP_011526453.1:n.2751+1083C>T
XM_011528152.1:c.2751+1083C>T XP_011526454.1:n.2751+1083C>T
XM_011528153.1:c.2856+65C>T XP_011526455.1:n.2856+65C>T
XR_936195.1:n.2917+65C>T
XR_936196.1:n.2812+1083C>T
XR_936197.1:n.2917+65C>T
XR_936198.1:n.2812+1083C>T
XM_006722804.3:c.54+919C>T XP_006722867.1:n.54+919C>T
NM_001367830.1:c.2823+65C>T NP_001354759.1:n.2823+65C>T
NM_020812.4:c.2718+1083C>T MANE Select NP_065863.2:n.2718+1083C>T