Canonical Allele Identifier: CA993518936

Gene: DOCK6

Linked Data

• dbSNP Id: rs2079558383
• gnomAD v3: 19-11220157-TTG-T
• gnomAD v4: 19-11220157-TTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11220159_11220160del , CM000681.2:g.11220159_11220160del	GRCh38
NC_000019.9:g.11330835_11330836del , CM000681.1:g.11330835_11330836del	GRCh37
NC_000019.8:g.11191835_11191836del	NCBI36
NG_031953.1:g.47334_47335del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587656.6:c.3655+1692_3655+1693del	ENSP00000468638.2:n.3655+1692_3655+1693del
ENST00000294618.12:c.3550+1692_3550+1693del MANE Select	ENSP00000294618.6:n.3550+1692_3550+1693del
ENST00000294618.11:c.3550+1692_3550+1693del	ENSP00000294618.6:n.3550+1692_3550+1693del
ENST00000587656.5:c.1415+1692_1415+1693del
NM_020812.3:c.3550+1692_3550+1693del	NP_065863.2:n.3550+1692_3550+1693del
XM_005260000.2:c.3748+1692_3748+1693del	XP_005260057.1:n.3748+1692_3748+1693del
XM_005260001.2:c.3655+1692_3655+1693del	XP_005260058.1:n.3655+1692_3655+1693del
XM_006722804.2:c.886+1692_886+1693del	XP_006722867.1:n.886+1692_886+1693del
XM_011528150.1:c.3688+1692_3688+1693del	XP_011526452.1:n.3688+1692_3688+1693del
XM_011528151.1:c.3676+1692_3676+1693del	XP_011526453.1:n.3676+1692_3676+1693del
XM_011528152.1:c.3583+1692_3583+1693del	XP_011526454.1:n.3583+1692_3583+1693del
XM_011528153.1:c.3688+1692_3688+1693del	XP_011526455.1:n.3688+1692_3688+1693del
XR_936195.1:n.3749+1692_3749+1693del
XR_936196.1:n.3766+1692_3766+1693del
XM_006722804.3:c.886+1692_886+1693del	XP_006722867.1:n.886+1692_886+1693del
NM_001367830.1:c.3655+1692_3655+1693del	NP_001354759.1:n.3655+1692_3655+1693del
NM_020812.4:c.3550+1692_3550+1693del MANE Select	NP_065863.2:n.3550+1692_3550+1693del