Canonical Allele Identifier: CA783268759

Gene: DOCK6

Linked Data

• dbSNP Id: rs1358139349
• MyVariant Identifiers: chr19:g.11342553_11342554insCATGCCT (hg19) ; chr19:g.11231877_11231878insCATGCCT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11231877_11231878insCATGCCT , CM000681.2:g.11231877_11231878insCATGCCT	GRCh38
NC_000019.9:g.11342553_11342554insCATGCCT , CM000681.1:g.11342553_11342554insCATGCCT	GRCh37
NC_000019.8:g.11203553_11203554insCATGCCT	NCBI36
NG_031953.1:g.35615_35616insAGGCATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587656.6:c.2823+307_2823+308insAGGCATG	ENSP00000468638.2:n.2823+307_2823+308insAGGCATG
ENST00000294618.12:c.2718+1325_2718+1326insAGGCATG MANE Select	ENSP00000294618.6:n.2718+1325_2718+1326insAGGCATG
ENST00000294618.11:c.2718+1325_2718+1326insAGGCATG	ENSP00000294618.6:n.2718+1325_2718+1326insAGGCATG
ENST00000585904.1:c.426+307_426+308insAGGCATG	ENSP00000465767.1:n.426+307_426+308insAGGCATG
ENST00000587656.5:c.583+307_583+308insAGGCATG
ENST00000590680.5:c.1061+1325_1061+1326insAGGCATG
NM_020812.3:c.2718+1325_2718+1326insAGGCATG	NP_065863.2:n.2718+1325_2718+1326insAGGCATG
XM_005260000.2:c.2823+307_2823+308insAGGCATG	XP_005260057.1:n.2823+307_2823+308insAGGCATG
XM_005260001.2:c.2823+307_2823+308insAGGCATG	XP_005260058.1:n.2823+307_2823+308insAGGCATG
XM_006722804.2:c.54+1161_54+1162insAGGCATG	XP_006722867.1:n.54+1161_54+1162insAGGCATG
XM_011528150.1:c.2856+307_2856+308insAGGCATG	XP_011526452.1:n.2856+307_2856+308insAGGCATG
XM_011528151.1:c.2751+1325_2751+1326insAGGCATG	XP_011526453.1:n.2751+1325_2751+1326insAGGCATG
XM_011528152.1:c.2751+1325_2751+1326insAGGCATG	XP_011526454.1:n.2751+1325_2751+1326insAGGCATG
XM_011528153.1:c.2856+307_2856+308insAGGCATG	XP_011526455.1:n.2856+307_2856+308insAGGCATG
XR_936195.1:n.2917+307_2917+308insAGGCATG
XR_936196.1:n.2812+1325_2812+1326insAGGCATG
XR_936197.1:n.2917+307_2917+308insAGGCATG
XR_936198.1:n.2812+1325_2812+1326insAGGCATG
XM_006722804.3:c.54+1161_54+1162insAGGCATG	XP_006722867.1:n.54+1161_54+1162insAGGCATG
NM_001367830.1:c.2823+307_2823+308insAGGCATG	NP_001354759.1:n.2823+307_2823+308insAGGCATG
NM_020812.4:c.2718+1325_2718+1326insAGGCATG MANE Select	NP_065863.2:n.2718+1325_2718+1326insAGGCATG