Canonical Allele Identifier: CA2813601501

Gene: DOCK6

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11231913_11231916dup , CM000681.2:g.11231913_11231916dup	GRCh38
NC_000019.9:g.11342589_11342592dup , CM000681.1:g.11342589_11342592dup	GRCh37
NC_000019.8:g.11203589_11203592dup	NCBI36
NG_031953.1:g.35579_35582dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587656.6:c.2823+271_2823+274dup	ENSP00000468638.2:n.2823+271_2823+274dup
ENST00000294618.12:c.2718+1289_2718+1292dup MANE Select	ENSP00000294618.6:n.2718+1289_2718+1292dup
ENST00000294618.11:c.2718+1289_2718+1292dup	ENSP00000294618.6:n.2718+1289_2718+1292dup
ENST00000585904.1:c.426+271_426+274dup	ENSP00000465767.1:n.426+271_426+274dup
ENST00000587656.5:c.583+271_583+274dup
ENST00000590680.5:c.1061+1289_1061+1292dup
NM_020812.3:c.2718+1289_2718+1292dup	NP_065863.2:n.2718+1289_2718+1292dup
XM_005260000.2:c.2823+271_2823+274dup	XP_005260057.1:n.2823+271_2823+274dup
XM_005260001.2:c.2823+271_2823+274dup	XP_005260058.1:n.2823+271_2823+274dup
XM_006722804.2:c.54+1125_54+1128dup	XP_006722867.1:n.54+1125_54+1128dup
XM_011528150.1:c.2856+271_2856+274dup	XP_011526452.1:n.2856+271_2856+274dup
XM_011528151.1:c.2751+1289_2751+1292dup	XP_011526453.1:n.2751+1289_2751+1292dup
XM_011528152.1:c.2751+1289_2751+1292dup	XP_011526454.1:n.2751+1289_2751+1292dup
XM_011528153.1:c.2856+271_2856+274dup	XP_011526455.1:n.2856+271_2856+274dup
XR_936195.1:n.2917+271_2917+274dup
XR_936196.1:n.2812+1289_2812+1292dup
XR_936197.1:n.2917+271_2917+274dup
XR_936198.1:n.2812+1289_2812+1292dup
XM_006722804.3:c.54+1125_54+1128dup	XP_006722867.1:n.54+1125_54+1128dup
NM_001367830.1:c.2823+271_2823+274dup	NP_001354759.1:n.2823+271_2823+274dup
NM_020812.4:c.2718+1289_2718+1292dup MANE Select	NP_065863.2:n.2718+1289_2718+1292dup