Canonical Allele Identifier: CA783268754

Gene: DOCK6

Linked Data

• dbSNP Id: rs1467137338
• MyVariant Identifiers: chr19:g.11342548_11342549insGCCAT (hg19) ; chr19:g.11231872_11231873insGCCAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11231873_11231874insCCATG , CM000681.2:g.11231873_11231874insCCATG	GRCh38
NC_000019.9:g.11342549_11342550insCCATG , CM000681.1:g.11342549_11342550insCCATG	GRCh37
NC_000019.8:g.11203549_11203550insCCATG	NCBI36
NG_031953.1:g.35620_35621insATGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587656.6:c.2823+312_2823+313insATGGC	ENSP00000468638.2:n.2823+312_2823+313insATGGC
ENST00000294618.12:c.2718+1330_2718+1331insATGGC MANE Select	ENSP00000294618.6:n.2718+1330_2718+1331insATGGC
ENST00000294618.11:c.2718+1330_2718+1331insATGGC	ENSP00000294618.6:n.2718+1330_2718+1331insATGGC
ENST00000585904.1:c.426+312_426+313insATGGC	ENSP00000465767.1:n.426+312_426+313insATGGC
ENST00000587656.5:c.583+312_583+313insATGGC
ENST00000590680.5:c.1061+1330_1061+1331insATGGC
NM_020812.3:c.2718+1330_2718+1331insATGGC	NP_065863.2:n.2718+1330_2718+1331insATGGC
XM_005260000.2:c.2823+312_2823+313insATGGC	XP_005260057.1:n.2823+312_2823+313insATGGC
XM_005260001.2:c.2823+312_2823+313insATGGC	XP_005260058.1:n.2823+312_2823+313insATGGC
XM_006722804.2:c.54+1166_54+1167insATGGC	XP_006722867.1:n.54+1166_54+1167insATGGC
XM_011528150.1:c.2856+312_2856+313insATGGC	XP_011526452.1:n.2856+312_2856+313insATGGC
XM_011528151.1:c.2751+1330_2751+1331insATGGC	XP_011526453.1:n.2751+1330_2751+1331insATGGC
XM_011528152.1:c.2751+1330_2751+1331insATGGC	XP_011526454.1:n.2751+1330_2751+1331insATGGC
XM_011528153.1:c.2856+312_2856+313insATGGC	XP_011526455.1:n.2856+312_2856+313insATGGC
XR_936195.1:n.2917+312_2917+313insATGGC
XR_936196.1:n.2812+1330_2812+1331insATGGC
XR_936197.1:n.2917+312_2917+313insATGGC
XR_936198.1:n.2812+1330_2812+1331insATGGC
XM_006722804.3:c.54+1166_54+1167insATGGC	XP_006722867.1:n.54+1166_54+1167insATGGC
NM_001367830.1:c.2823+312_2823+313insATGGC	NP_001354759.1:n.2823+312_2823+313insATGGC
NM_020812.4:c.2718+1330_2718+1331insATGGC MANE Select	NP_065863.2:n.2718+1330_2718+1331insATGGC