Canonical Allele Identifier: CA2322831842
Gene: DOCK6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11231857_11231858delinsCA , CM000681.2:g.11231857_11231858delinsCA GRCh38
NC_000019.9:g.11342533_11342534delinsCA , CM000681.1:g.11342533_11342534delinsCA GRCh37
NC_000019.8:g.11203533_11203534delinsCA NCBI36
NG_031953.1:g.35635_35636delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000587656.6:c.2823+327_2823+328delinsTG ENSP00000468638.2:n.2823+327_2823+328delinsTG
ENST00000294618.12:c.2718+1345_2718+1346delinsTG MANE Select ENSP00000294618.6:n.2718+1345_2718+1346delinsTG
ENST00000294618.11:c.2718+1345_2718+1346delinsTG ENSP00000294618.6:n.2718+1345_2718+1346delinsTG
ENST00000585904.1:c.426+327_426+328delinsTG ENSP00000465767.1:n.426+327_426+328delinsTG
ENST00000587656.5:c.583+327_583+328delinsTG
ENST00000590680.5:c.1061+1345_1061+1346delinsTG
NM_020812.3:c.2718+1345_2718+1346delinsTG NP_065863.2:n.2718+1345_2718+1346delinsTG
XM_005260000.2:c.2823+327_2823+328delinsTG XP_005260057.1:n.2823+327_2823+328delinsTG
XM_005260001.2:c.2823+327_2823+328delinsTG XP_005260058.1:n.2823+327_2823+328delinsTG
XM_006722804.2:c.54+1181_54+1182delinsTG XP_006722867.1:n.54+1181_54+1182delinsTG
XM_011528150.1:c.2856+327_2856+328delinsTG XP_011526452.1:n.2856+327_2856+328delinsTG
XM_011528151.1:c.2751+1345_2751+1346delinsTG XP_011526453.1:n.2751+1345_2751+1346delinsTG
XM_011528152.1:c.2751+1345_2751+1346delinsTG XP_011526454.1:n.2751+1345_2751+1346delinsTG
XM_011528153.1:c.2856+327_2856+328delinsTG XP_011526455.1:n.2856+327_2856+328delinsTG
XR_936195.1:n.2917+327_2917+328delinsTG
XR_936196.1:n.2812+1345_2812+1346delinsTG
XR_936197.1:n.2917+327_2917+328delinsTG
XR_936198.1:n.2812+1345_2812+1346delinsTG
XM_006722804.3:c.54+1181_54+1182delinsTG XP_006722867.1:n.54+1181_54+1182delinsTG
NM_001367830.1:c.2823+327_2823+328delinsTG NP_001354759.1:n.2823+327_2823+328delinsTG
NM_020812.4:c.2718+1345_2718+1346delinsTG MANE Select NP_065863.2:n.2718+1345_2718+1346delinsTG