Canonical Allele Identifier: CA783256099

Gene: DOCK6

Linked Data

• dbSNP Id: rs1364717716
• MyVariant Identifiers: chr19:g.11343089_11343090insA (hg19) ; chr19:g.11232413_11232414insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11232418dup , CM000681.2:g.11232418dup	GRCh38
NC_000019.9:g.11343094dup , CM000681.1:g.11343094dup	GRCh37
NC_000019.8:g.11204094dup	NCBI36
NG_031953.1:g.35079dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587656.6:c.2719-125dup	ENSP00000468638.2:n.2719-125dup
ENST00000294618.12:c.2718+789dup MANE Select	ENSP00000294618.6:n.2718+789dup
ENST00000294618.11:c.2718+789dup	ENSP00000294618.6:n.2718+789dup
ENST00000585904.1:c.322-125dup	ENSP00000465767.1:n.322-125dup
ENST00000587656.5:c.479-125dup
ENST00000590680.5:c.1061+789dup
NM_020812.3:c.2718+789dup	NP_065863.2:n.2718+789dup
XM_005260000.2:c.2719-125dup	XP_005260057.1:n.2719-125dup
XM_005260001.2:c.2719-125dup	XP_005260058.1:n.2719-125dup
XM_006722804.2:c.54+625dup	XP_006722867.1:n.54+625dup
XM_011528150.1:c.2752-125dup	XP_011526452.1:n.2752-125dup
XM_011528151.1:c.2751+789dup	XP_011526453.1:n.2751+789dup
XM_011528152.1:c.2751+789dup	XP_011526454.1:n.2751+789dup
XM_011528153.1:c.2752-125dup	XP_011526455.1:n.2752-125dup
XR_936195.1:n.2813-125dup
XR_936196.1:n.2812+789dup
XR_936197.1:n.2813-125dup
XR_936198.1:n.2812+789dup
XM_006722804.3:c.54+625dup	XP_006722867.1:n.54+625dup
NM_001367830.1:c.2719-125dup	NP_001354759.1:n.2719-125dup
NM_020812.4:c.2718+789dup MANE Select	NP_065863.2:n.2718+789dup