Canonical Allele Identifier: CA2813601523

Gene: DOCK6

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11232214dup , CM000681.2:g.11232214dup	GRCh38
NC_000019.9:g.11342890dup , CM000681.1:g.11342890dup	GRCh37
NC_000019.8:g.11203890dup	NCBI36
NG_031953.1:g.35283dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587656.6:c.2798dup	ENSP00000468638.2:p.Tyr934LeufsTer?
ENST00000294618.12:c.2718+993dup MANE Select	ENSP00000294618.6:n.2718+993dup
ENST00000294618.11:c.2718+993dup	ENSP00000294618.6:n.2718+993dup
ENST00000585904.1:c.401dup	ENSP00000465767.1:p.Tyr135LeufsTer15
ENST00000587656.5:c.558dup
ENST00000590680.5:c.1061+993dup
NM_020812.3:c.2718+993dup	NP_065863.2:n.2718+993dup
XM_005260000.2:c.2798dup	XP_005260057.1:p.Tyr934LeufsTer15
XM_005260001.2:c.2798dup	XP_005260058.1:p.Tyr934LeufsTer?
XM_006722804.2:c.54+829dup	XP_006722867.1:n.54+829dup
XM_011528150.1:c.2831dup	XP_011526452.1:p.Tyr945LeufsTer?
XM_011528151.1:c.2751+993dup	XP_011526453.1:n.2751+993dup
XM_011528152.1:c.2751+993dup	XP_011526454.1:n.2751+993dup
XM_011528153.1:c.2831dup	XP_011526455.1:p.Tyr945LeufsTer?
XR_936195.1:n.2892dup
XR_936196.1:n.2812+993dup
XR_936197.1:n.2892dup
XR_936198.1:n.2812+993dup
XM_006722804.3:c.54+829dup	XP_006722867.1:n.54+829dup
NM_001367830.1:c.2798dup	NP_001354759.1:p.Tyr934LeufsTer?
NM_020812.4:c.2718+993dup MANE Select	NP_065863.2:n.2718+993dup