Canonical Allele Identifier: CA2582496302
Gene: DOCK6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11232055_11232058del , CM000681.2:g.11232055_11232058del GRCh38
NC_000019.9:g.11342731_11342734del , CM000681.1:g.11342731_11342734del GRCh37
NC_000019.8:g.11203731_11203734del NCBI36
NG_031953.1:g.35439_35442del

Transcript Alleles

HGVS Amino-acid Change
ENST00000587656.6:c.2823+131_2823+134del ENSP00000468638.2:n.2823+131_2823+134del
ENST00000294618.12:c.2718+1149_2718+1152del MANE Select ENSP00000294618.6:n.2718+1149_2718+1152del
ENST00000294618.11:c.2718+1149_2718+1152del ENSP00000294618.6:n.2718+1149_2718+1152del
ENST00000585904.1:c.426+131_426+134del ENSP00000465767.1:n.426+131_426+134del
ENST00000587656.5:c.583+131_583+134del
ENST00000590680.5:c.1061+1149_1061+1152del
NM_020812.3:c.2718+1149_2718+1152del NP_065863.2:n.2718+1149_2718+1152del
XM_005260000.2:c.2823+131_2823+134del XP_005260057.1:n.2823+131_2823+134del
XM_005260001.2:c.2823+131_2823+134del XP_005260058.1:n.2823+131_2823+134del
XM_006722804.2:c.54+985_54+988del XP_006722867.1:n.54+985_54+988del
XM_011528150.1:c.2856+131_2856+134del XP_011526452.1:n.2856+131_2856+134del
XM_011528151.1:c.2751+1149_2751+1152del XP_011526453.1:n.2751+1149_2751+1152del
XM_011528152.1:c.2751+1149_2751+1152del XP_011526454.1:n.2751+1149_2751+1152del
XM_011528153.1:c.2856+131_2856+134del XP_011526455.1:n.2856+131_2856+134del
XR_936195.1:n.2917+131_2917+134del
XR_936196.1:n.2812+1149_2812+1152del
XR_936197.1:n.2917+131_2917+134del
XR_936198.1:n.2812+1149_2812+1152del
XM_006722804.3:c.54+985_54+988del XP_006722867.1:n.54+985_54+988del
NM_001367830.1:c.2823+131_2823+134del NP_001354759.1:n.2823+131_2823+134del
NM_020812.4:c.2718+1149_2718+1152del MANE Select NP_065863.2:n.2718+1149_2718+1152del